2,800 Clinical Research Professional jobs in the United States
Clinical Research Professional
80017 Aurora, Colorado
University of Colorado
Posted 2 days ago
Job Viewed
Job Description
**Clinical Research Professional**
**Description**
**University of Colorado Anschutz Medical Campus**
**Department: Anna and John J. Sie Center for Down Syndrome, Children's Hospital Colorado**
**Job Title:**
**Position #:** **- Requisition #:37574**
**Job Summary:**
Key Responsibilities:
+ Act as a Primary Coordinator on multiple trials/studies, managing the day-to-day operations.
+ Develop protocol-specific source documents and organize and prepare research materials for research study visits.
+ Lead participant recruitment, communication, and scheduling.
+ Administer developmental assessments and conduct study interviews.
+ Responsible for data management for all clinical trial data. Collect, code, and analyze data obtained from research in an accurate and timely manner.
+ Review and resolve data discrepancies in data management systems.
+ Accurately and timely enter clinical trials data into centralized data management systems, ensure data quality, and review participant records for completeness, accuracy, and quality.
+ Independently perform study-related processes, procedures, and assessments as defined in the study protocol and in compliance with regulating bodies.
+ Assist Team Leads, Supervisors, and/or management with the creation and implementation of processes and procedures and quality improvement initiatives.
+ Participate in subject recruitment efforts, including communicating with patients expressing an interest and all pre-screening/screening activities.
+ Complete regulatory maintenance of assigned clinical trials (IRB and FDA initial submissions, amendments, continuing reviews, etc.).
**Work Location:**
On-site
**Why Join Us:**
+ Multiple Sie Center studies were used to create the 2022 American Academy of Pediatrics Down Syndrome Guidelines.
+ Establish standardized medical and developmental references.
+ Develop best practices, medical testing, and procedures.
+ Improve the identification and treatment of complex comorbidities.
+ Create tangible support resources for children and families.
+ Identify biomarkers to improve diagnoses and reduce costs.
+ Improve access to care for the high-risk, underserved Spanish-speaking population.
**Why work for the University?**
+ Medical: Multiple plan options
+ Dental: Multiple plan options
+ Additional Insurance: Disability, Life, Vision
+ Retirement 401(a) Plan: Employer contributes 10% of your gross pay
+ Paid Time Off: Accruals over the year
+ Vacation Days: 22/year (maximum accrual 352 hours)
+ Sick Days: 15/year (unlimited maximum accrual)
+ Holiday Days: 10/year
+ Tuition Benefit: Employees have access to this benefit on all CU campuses
+ ECO Pass: Reduced-rate RTD Bus and light rail service
**Qualifications:**
**Minimum Qualifications:**
+ Bachelor's degree in any field.
+ **Substitution:** A combination of education and related technical/paraprofessional experience may be substituted for the bachelor's degree on a year-for-year basis.
+ One (1) year of clinical research or related experience.
**Applicants must meet minimum qualifications at the time of hire.**
**Condition of Employment:**
+ Must successfully pass a drug test through Children's Hospital Colorado.*
+ _Must be willing and able to pass a national criminal background check._
_*For questions regarding Children's Hospital drug testing requirements, please contact Children's Human Resources at . Some positions may require testing if access to the Children's Hospital or their systems is needed at any time during employment with the University. If drug testing is required, it will be listed in the job posting._
**_Preferred Qualifications:_**
+ _Bachelor's degree in science or a health-related field._
+ _Two (2) years of clinical research or related experience._
+ _Experience with electronic data capture systems (e.g., EMR or EHR and data management systems)._
**_Knowledge, Skills, and Abilities:_**
+ _Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)._
+ _Ability to communicate effectively, both in writing and orally._
+ _Ability to establish and maintain effective working relationships with employees at all levels throughout the institution._
+ _Outstanding customer service skills._
+ _Knowledge of basic human anatomy, physiology, and medical terminology._
+ _Ability to interpret and master complex research protocol information._
+ _Ability to multitask and meet deadlines._
+ _Ability to proactively identify and solve problems._
+ _Demonstrated initiative and strong follow-through skills._
**_How to Apply:_**
_For full consideration, please submit the following document(s):_
_1. A letter of interest describing relevant job experiences as they relate to the listed job qualifications and interest in the position._
_2. Curriculum vitae / Resume._
_3. Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address._
_Questions should be directed to: Kristine Wolter-Warmerdam, ( of Applications Begins:_**
_Immediately and continues until the position is filled. For best consideration, apply by August 29, 2025._
**_Anticipated Pay Range:_**
_The hiring range for this position has been established as $52,721 to $67,061._
_The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. This position may be eligible for overtime compensation, depending on the level._
_Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave, health plans, and retirement contributions that add to your bottom line._
_Total Compensation Calculator: ( Employment Opportunity Statement:_**
_The University of Colorado (CU) is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing non-discrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply, including protected veterans and individuals with disabilities._
**_ADA Statement:_**
_The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at ( ._
**_Background Check Statement:_**
_The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students, and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees._
**_Vaccination Statement:_**
_CU Anschutz strongly encourages vaccination against the COVID-19 virus and other vaccine-preventable diseases ( . If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety-sensitive job duties, you must enroll in the occupational health medical surveillance program ( ._
_Application Materials Required: Cover Letter, Resume/CV, List of References_ **_Job Category_**
_: Research Services_ **_Primary Location_**
_: Aurora Department: U0001 -- Anschutz Med Campus or Denver - 20269 - SOM-PEDS GENERAL OPERATIONS_ **_Schedule_**
_: Full-time_ **_Posting Date_**
_: Aug 18, 2025_ **_Unposting Date_**
_: Ongoing Posting Contact Name: Kristine Wolter-Warmerdam Posting Contact Email: ( Position Number: _
**_To apply, visit ( 2025 Jobelephant.com Inc. All rights reserved._
_Posted by the FREE value-added recruitment advertising agency ( Research Professional - 37574 University Staff
Established in 2010, the Anna and John J. Sie Center for Down Syndrome at Children's Hospital Colorado is one of the leading Down syndrome clinics in the United States. Our world-renowned team of experts provides medical, educational, and therapeutic care that helps children and adolescents with Down syndrome thrive. Through close partnership and collaboration with the Global Down Syndrome Foundation and Linda Crnic Research Institute, the Sie Center is a model for Down syndrome care, combining excellence in clinical care, research, community engagement, advocacy, and education.In the first 14 years, the Sie Center has served over 2,500 patients from 32 states, Puerto Rico, and 11 countries. Our pediatric specialists work together to provide the best possible collaborative care for children with Down syndrome using a multidisciplinary team-based approach. Our services include evaluation, consultation, and therapies for infants, children, teens, and young adults through the age of 22.This position will support two clinical trials - Birthday-Early Development in Down Syndrome and CAPEabilities (Communication and Play Early Abilities in Children with Down Syndrome). These trials focus on the developmental, behavioral, and biomedical factors impacting young children with Down syndrome.
- this role is expected to work onsite and is located in Aurora, CO.
In just 14 years, the Sie Center has become one of the leading medical clinics for the pediatric population with Down syndrome. Our innovative care directly improves not only the lives and clinical care of our own patients and families, but through our clinical research, extends nationally and globally to set new standards for children and young adults with Down syndrome, including:The mission of the Sie Center for Down Syndrome research program is to improve the quality of care and life of children and young adults with Down syndrome.We accomplish this by serving as a model of multidisciplinary collaboration through the synthesis of our medical, behavioral, mental health, therapy, and educational expertise, as well as our partnership with internal and external investigators.We have AMAZING benefits and offerexceptional amounts of holiday, vacation, and sick leave! The University of Colorado offers an excellent benefits package, including:There are many additional perks & programs with the CU Advantage ( .
The University of Colorado does not discriminate on the basis of race, color, national origin, sex, age, pregnancy, disability, creed, religion, sexual orientation, gender identity, gender expression, veteran status, political affiliation, or political philosophy. All qualified individuals are encouraged to apply.
**Description**
**University of Colorado Anschutz Medical Campus**
**Department: Anna and John J. Sie Center for Down Syndrome, Children's Hospital Colorado**
**Job Title:**
**Position #:** **- Requisition #:37574**
**Job Summary:**
Key Responsibilities:
+ Act as a Primary Coordinator on multiple trials/studies, managing the day-to-day operations.
+ Develop protocol-specific source documents and organize and prepare research materials for research study visits.
+ Lead participant recruitment, communication, and scheduling.
+ Administer developmental assessments and conduct study interviews.
+ Responsible for data management for all clinical trial data. Collect, code, and analyze data obtained from research in an accurate and timely manner.
+ Review and resolve data discrepancies in data management systems.
+ Accurately and timely enter clinical trials data into centralized data management systems, ensure data quality, and review participant records for completeness, accuracy, and quality.
+ Independently perform study-related processes, procedures, and assessments as defined in the study protocol and in compliance with regulating bodies.
+ Assist Team Leads, Supervisors, and/or management with the creation and implementation of processes and procedures and quality improvement initiatives.
+ Participate in subject recruitment efforts, including communicating with patients expressing an interest and all pre-screening/screening activities.
+ Complete regulatory maintenance of assigned clinical trials (IRB and FDA initial submissions, amendments, continuing reviews, etc.).
**Work Location:**
On-site
**Why Join Us:**
+ Multiple Sie Center studies were used to create the 2022 American Academy of Pediatrics Down Syndrome Guidelines.
+ Establish standardized medical and developmental references.
+ Develop best practices, medical testing, and procedures.
+ Improve the identification and treatment of complex comorbidities.
+ Create tangible support resources for children and families.
+ Identify biomarkers to improve diagnoses and reduce costs.
+ Improve access to care for the high-risk, underserved Spanish-speaking population.
**Why work for the University?**
+ Medical: Multiple plan options
+ Dental: Multiple plan options
+ Additional Insurance: Disability, Life, Vision
+ Retirement 401(a) Plan: Employer contributes 10% of your gross pay
+ Paid Time Off: Accruals over the year
+ Vacation Days: 22/year (maximum accrual 352 hours)
+ Sick Days: 15/year (unlimited maximum accrual)
+ Holiday Days: 10/year
+ Tuition Benefit: Employees have access to this benefit on all CU campuses
+ ECO Pass: Reduced-rate RTD Bus and light rail service
**Qualifications:**
**Minimum Qualifications:**
+ Bachelor's degree in any field.
+ **Substitution:** A combination of education and related technical/paraprofessional experience may be substituted for the bachelor's degree on a year-for-year basis.
+ One (1) year of clinical research or related experience.
**Applicants must meet minimum qualifications at the time of hire.**
**Condition of Employment:**
+ Must successfully pass a drug test through Children's Hospital Colorado.*
+ _Must be willing and able to pass a national criminal background check._
_*For questions regarding Children's Hospital drug testing requirements, please contact Children's Human Resources at . Some positions may require testing if access to the Children's Hospital or their systems is needed at any time during employment with the University. If drug testing is required, it will be listed in the job posting._
**_Preferred Qualifications:_**
+ _Bachelor's degree in science or a health-related field._
+ _Two (2) years of clinical research or related experience._
+ _Experience with electronic data capture systems (e.g., EMR or EHR and data management systems)._
**_Knowledge, Skills, and Abilities:_**
+ _Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)._
+ _Ability to communicate effectively, both in writing and orally._
+ _Ability to establish and maintain effective working relationships with employees at all levels throughout the institution._
+ _Outstanding customer service skills._
+ _Knowledge of basic human anatomy, physiology, and medical terminology._
+ _Ability to interpret and master complex research protocol information._
+ _Ability to multitask and meet deadlines._
+ _Ability to proactively identify and solve problems._
+ _Demonstrated initiative and strong follow-through skills._
**_How to Apply:_**
_For full consideration, please submit the following document(s):_
_1. A letter of interest describing relevant job experiences as they relate to the listed job qualifications and interest in the position._
_2. Curriculum vitae / Resume._
_3. Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address._
_Questions should be directed to: Kristine Wolter-Warmerdam, ( of Applications Begins:_**
_Immediately and continues until the position is filled. For best consideration, apply by August 29, 2025._
**_Anticipated Pay Range:_**
_The hiring range for this position has been established as $52,721 to $67,061._
_The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. This position may be eligible for overtime compensation, depending on the level._
_Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave, health plans, and retirement contributions that add to your bottom line._
_Total Compensation Calculator: ( Employment Opportunity Statement:_**
_The University of Colorado (CU) is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing non-discrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply, including protected veterans and individuals with disabilities._
**_ADA Statement:_**
_The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at ( ._
**_Background Check Statement:_**
_The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students, and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees._
**_Vaccination Statement:_**
_CU Anschutz strongly encourages vaccination against the COVID-19 virus and other vaccine-preventable diseases ( . If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety-sensitive job duties, you must enroll in the occupational health medical surveillance program ( ._
_Application Materials Required: Cover Letter, Resume/CV, List of References_ **_Job Category_**
_: Research Services_ **_Primary Location_**
_: Aurora Department: U0001 -- Anschutz Med Campus or Denver - 20269 - SOM-PEDS GENERAL OPERATIONS_ **_Schedule_**
_: Full-time_ **_Posting Date_**
_: Aug 18, 2025_ **_Unposting Date_**
_: Ongoing Posting Contact Name: Kristine Wolter-Warmerdam Posting Contact Email: ( Position Number: _
**_To apply, visit ( 2025 Jobelephant.com Inc. All rights reserved._
_Posted by the FREE value-added recruitment advertising agency ( Research Professional - 37574 University Staff
Established in 2010, the Anna and John J. Sie Center for Down Syndrome at Children's Hospital Colorado is one of the leading Down syndrome clinics in the United States. Our world-renowned team of experts provides medical, educational, and therapeutic care that helps children and adolescents with Down syndrome thrive. Through close partnership and collaboration with the Global Down Syndrome Foundation and Linda Crnic Research Institute, the Sie Center is a model for Down syndrome care, combining excellence in clinical care, research, community engagement, advocacy, and education.In the first 14 years, the Sie Center has served over 2,500 patients from 32 states, Puerto Rico, and 11 countries. Our pediatric specialists work together to provide the best possible collaborative care for children with Down syndrome using a multidisciplinary team-based approach. Our services include evaluation, consultation, and therapies for infants, children, teens, and young adults through the age of 22.This position will support two clinical trials - Birthday-Early Development in Down Syndrome and CAPEabilities (Communication and Play Early Abilities in Children with Down Syndrome). These trials focus on the developmental, behavioral, and biomedical factors impacting young children with Down syndrome.
- this role is expected to work onsite and is located in Aurora, CO.
In just 14 years, the Sie Center has become one of the leading medical clinics for the pediatric population with Down syndrome. Our innovative care directly improves not only the lives and clinical care of our own patients and families, but through our clinical research, extends nationally and globally to set new standards for children and young adults with Down syndrome, including:The mission of the Sie Center for Down Syndrome research program is to improve the quality of care and life of children and young adults with Down syndrome.We accomplish this by serving as a model of multidisciplinary collaboration through the synthesis of our medical, behavioral, mental health, therapy, and educational expertise, as well as our partnership with internal and external investigators.We have AMAZING benefits and offerexceptional amounts of holiday, vacation, and sick leave! The University of Colorado offers an excellent benefits package, including:There are many additional perks & programs with the CU Advantage ( .
The University of Colorado does not discriminate on the basis of race, color, national origin, sex, age, pregnancy, disability, creed, religion, sexual orientation, gender identity, gender expression, veteran status, political affiliation, or political philosophy. All qualified individuals are encouraged to apply.
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0
Clinical Research Professional I
72205 Little Rock, Arkansas
Arkansas Children's
Posted 2 days ago
Job Viewed
Job Description
**Work Shift:**
Please see job description for details.
**Time Type:**
Full time
**Department:**
CC Food Allergy Gen Research Acct
**Summary:**
The Clinical Research Professional I coordinates selected specific aspects of clinical research studies.
This role serves as a resource for research study participants, families, other healthcare providers, and members of the clinical research team regarding specified aspects of the study.
**Additional Information:**
**Required Education:**
High school diploma or GED or equivalent
**Recommended Education:**
Bachelor's degree in a related field of study.
**Required Work Experience:**
High School Diploma/GED, or 2 years of experience in lieu of a diploma/GED.
**Recommended Work Experience:**
**Required Certifications:**
**Recommended Certifications:**
Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals, Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates
**Description**
1. Recruits and screens patients for enrollment eligibility and participation in research projects. Obtains consent for participation in accordance with all government regulations and internal policies/procedures.
2. Prepares flowcharts, study specific source documents, and collects/records subject data on case report forms. Creates databases and performs date entry into the database.
3. Serves as a research resource to subjects, families, and other healthcare providers regarding the needs of study and subjects family preserving patient/subject privacy and maintaining confidentiality of subject information.
4. Promotes knowledge of current professional practice and research standards, laws and regulations that affect human subjects research.
5. Facilitates and improves collaboration with other departments to facilitate research across the continuum.
6. Coordinates/collects requested data for sponsor review during site visits. Assists study monitor(s) in chart and case report form review.
7. Maintains files and study documentation according to institutional and regulatory standards
8. Performs other duties as assigned.
Arkansas Children's ( is the only hospital system in the state dedicated to caring for children, which enables us to uniquely shape the landscape of pediatric care in Arkansas.
Arkansas Children's is driven by four core values-safety, teamwork, compassion and excellence-which inform every action.
Arkansas Children's Hospital has received Magnet Status ( from the American Nurses Credentialing Center (ANCC), for nursing excellence and patient outcomes. And we are nationally ranked by U.S. News & World Report ( for Cancer, Cardiology & Heart Surgery, Diabetes & Endocrinology, Nephrology, Neurology & Neurosurgery, Pulmonology & Lung Surgery and Urology.
For more than a century, Arkansas Children's has met the unique needs of children. But we're more than just a hospital treating sick kids-our services include two hospitals, a pediatric research institute, foundation, clinics, education and outreach, all with an unyielding commitment to making children better today and healthier tomorrow.
Arkansas Children's Little Rock campus includes a 336-bed hospital with the state's only pediatric Level 1 Trauma Center, burn center, Level 4 neonatal intensive care and pediatric intensive care, as well as a nationally-recognized transport service. And Arkansas Children's Northwest ( provides inpatient and emergency care, clinic rooms and diagnostic services to children in that corner of the state.
_"Arkansas Children's is a place of hope and comfort for children and parents. When you are at children's, you are part of an elite team united with a common goal of saving children and making their lives better."_ Michael - Business Operations Manager
"Arkansas Children's Hospital is a prestigious institution that cares for children." Linda - Information Systems Analyst
"We are an organization of care, love, and hope while we champion children." Angela - Parking and Fleet Coordinator
"Care, love, and hope for children!" Kathy - Administrative Assistant
"When I think of my time here at Arkansas Children's Hospital, I can honestly say that it has given me a unique perspective on the human condition, and the various roles that we all have in patient care. As a supply assistant, I have a very important job ensuring that the doctors and nurses have what they need to provide the world class medical care to the Children of Arkansas and surrounding states. Being a Champion for Children is more than a catch phrase, it is a way of life!" Nick - Supply Assistant
Arkansas Children's provides equal employment opportunity to all persons without regard to age, race, color, religion, national origin or citizenship status, disability, military status, sexual orientation, gender identity or expression, pregnancy or any other category protected by federal, state and local laws. Further, Arkansas Children's will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.
Please see job description for details.
**Time Type:**
Full time
**Department:**
CC Food Allergy Gen Research Acct
**Summary:**
The Clinical Research Professional I coordinates selected specific aspects of clinical research studies.
This role serves as a resource for research study participants, families, other healthcare providers, and members of the clinical research team regarding specified aspects of the study.
**Additional Information:**
**Required Education:**
High school diploma or GED or equivalent
**Recommended Education:**
Bachelor's degree in a related field of study.
**Required Work Experience:**
High School Diploma/GED, or 2 years of experience in lieu of a diploma/GED.
**Recommended Work Experience:**
**Required Certifications:**
**Recommended Certifications:**
Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals, Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates
**Description**
1. Recruits and screens patients for enrollment eligibility and participation in research projects. Obtains consent for participation in accordance with all government regulations and internal policies/procedures.
2. Prepares flowcharts, study specific source documents, and collects/records subject data on case report forms. Creates databases and performs date entry into the database.
3. Serves as a research resource to subjects, families, and other healthcare providers regarding the needs of study and subjects family preserving patient/subject privacy and maintaining confidentiality of subject information.
4. Promotes knowledge of current professional practice and research standards, laws and regulations that affect human subjects research.
5. Facilitates and improves collaboration with other departments to facilitate research across the continuum.
6. Coordinates/collects requested data for sponsor review during site visits. Assists study monitor(s) in chart and case report form review.
7. Maintains files and study documentation according to institutional and regulatory standards
8. Performs other duties as assigned.
Arkansas Children's ( is the only hospital system in the state dedicated to caring for children, which enables us to uniquely shape the landscape of pediatric care in Arkansas.
Arkansas Children's is driven by four core values-safety, teamwork, compassion and excellence-which inform every action.
Arkansas Children's Hospital has received Magnet Status ( from the American Nurses Credentialing Center (ANCC), for nursing excellence and patient outcomes. And we are nationally ranked by U.S. News & World Report ( for Cancer, Cardiology & Heart Surgery, Diabetes & Endocrinology, Nephrology, Neurology & Neurosurgery, Pulmonology & Lung Surgery and Urology.
For more than a century, Arkansas Children's has met the unique needs of children. But we're more than just a hospital treating sick kids-our services include two hospitals, a pediatric research institute, foundation, clinics, education and outreach, all with an unyielding commitment to making children better today and healthier tomorrow.
Arkansas Children's Little Rock campus includes a 336-bed hospital with the state's only pediatric Level 1 Trauma Center, burn center, Level 4 neonatal intensive care and pediatric intensive care, as well as a nationally-recognized transport service. And Arkansas Children's Northwest ( provides inpatient and emergency care, clinic rooms and diagnostic services to children in that corner of the state.
_"Arkansas Children's is a place of hope and comfort for children and parents. When you are at children's, you are part of an elite team united with a common goal of saving children and making their lives better."_ Michael - Business Operations Manager
"Arkansas Children's Hospital is a prestigious institution that cares for children." Linda - Information Systems Analyst
"We are an organization of care, love, and hope while we champion children." Angela - Parking and Fleet Coordinator
"Care, love, and hope for children!" Kathy - Administrative Assistant
"When I think of my time here at Arkansas Children's Hospital, I can honestly say that it has given me a unique perspective on the human condition, and the various roles that we all have in patient care. As a supply assistant, I have a very important job ensuring that the doctors and nurses have what they need to provide the world class medical care to the Children of Arkansas and surrounding states. Being a Champion for Children is more than a catch phrase, it is a way of life!" Nick - Supply Assistant
Arkansas Children's provides equal employment opportunity to all persons without regard to age, race, color, religion, national origin or citizenship status, disability, military status, sexual orientation, gender identity or expression, pregnancy or any other category protected by federal, state and local laws. Further, Arkansas Children's will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.
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1
Medical Research Associate
78284 San Antonio, Texas
ICON Clinical Research
Posted 8 days ago
Job Viewed
Job Description
Research Assistant(Certified Phlebotomist/Medical Assistant/CNA/Paramedic)- ICON San Antonio TX - As Needed M-F Day Shift
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Research Assistant to join our diverse and dynamic team. As a Research Assistant at ICON, you will support the design, execution, and management of clinical trials and research studies. You will play a crucial role in ensuring the accuracy and quality of data collection and analysis, contributing to the success of innovative treatments and therapies.
**Title:** Research Assistant (Phlebotomist/CMA/CNA)
**Job Type:** PRN/ As Needed
**Shift/Schedule:** M-F Day Shift 6 AM-230 PM
**Location:** 100% on site San Antonio TX
**What You Will Be Doing:**
+ Assisting in the planning and execution of clinical trials and research studies, including data collection and management.
+ Supporting the research team with literature reviews, data entry, and analysis to inform study protocols and findings.
+ Maintaining accurate and organized research documentation, ensuring compliance with regulatory and ethical standards.
+ Collaborating with cross-functional teams to ensure timely completion of research tasks and adherence to study timelines.
+ Assisting with the preparation of research reports, manuscripts, and presentations for internal and external stakeholders.
**Your Profile:**
+ High School Diploma or equivalency with medical assistant training/certification or other allied health certification
+ Medical Assistant, Phlebotomy Technician, Paramedic, EMT, OR LVN preferably with two years of experience
+ Strong organizational and time management skills, with attention to detail in data collection and documentation.
+ Proficiency with research software and tools for data entry, analysis, and reporting.
+ Excellent communication and teamwork skills, with the ability to work collaboratively with researchers and other stakeholders.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Research Assistant to join our diverse and dynamic team. As a Research Assistant at ICON, you will support the design, execution, and management of clinical trials and research studies. You will play a crucial role in ensuring the accuracy and quality of data collection and analysis, contributing to the success of innovative treatments and therapies.
**Title:** Research Assistant (Phlebotomist/CMA/CNA)
**Job Type:** PRN/ As Needed
**Shift/Schedule:** M-F Day Shift 6 AM-230 PM
**Location:** 100% on site San Antonio TX
**What You Will Be Doing:**
+ Assisting in the planning and execution of clinical trials and research studies, including data collection and management.
+ Supporting the research team with literature reviews, data entry, and analysis to inform study protocols and findings.
+ Maintaining accurate and organized research documentation, ensuring compliance with regulatory and ethical standards.
+ Collaborating with cross-functional teams to ensure timely completion of research tasks and adherence to study timelines.
+ Assisting with the preparation of research reports, manuscripts, and presentations for internal and external stakeholders.
**Your Profile:**
+ High School Diploma or equivalency with medical assistant training/certification or other allied health certification
+ Medical Assistant, Phlebotomy Technician, Paramedic, EMT, OR LVN preferably with two years of experience
+ Strong organizational and time management skills, with attention to detail in data collection and documentation.
+ Proficiency with research software and tools for data entry, analysis, and reporting.
+ Excellent communication and teamwork skills, with the ability to work collaboratively with researchers and other stakeholders.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
View Now
2
Medical Research Associate
78284 San Antonio, Texas
ICON Clinical Research
Posted 16 days ago
Job Viewed
Job Description
Research Assistant(Phlebotomist/Medical Assistant)- Full Time- Weekend Day Shift - ICON San Antonio TX
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As an MRA at ICON, you will support the design, execution, and management of clinical trials and research studies. You will play a crucial role in ensuring the accuracy and quality of data collection and analysis, contributing to the success of innovative treatments and therapies.
**Title:** Medical Research Associate (Phlebotomist/CMA/CNA)
**Job Type** : Full Time/Permanent
**Shift/Schedule:** Friday-Sunday Day Shift
**Location** : 100% on site San Antonio TX
**What You Will Be Doing:**
+ Assisting in the planning and execution of clinical trials and research studies, including data collection and management.
+ Supporting the research team with literature reviews, data entry, and analysis to inform study protocols and findings.
+ Maintaining accurate and organized research documentation, ensuring compliance with regulatory and ethical standards.
+ Collaborating with cross-functional teams to ensure timely completion of research tasks and adherence to study timelines.
+ Assisting with the preparation of research reports, manuscripts, and presentations for internal and external stakeholders.
**Your Profile:**
+ High School Diploma or equivalency with medical assistant training/certification or other allied health certification
+ Medical Assistant, Phlebotomy Technician, Paramedic, EMT, OR LVN preferably with two years of experience
+ Strong organizational and time management skills, with attention to detail in data collection and documentation.
+ Proficiency with research software and tools for data entry, analysis, and reporting.
+ Excellent communication and teamwork skills, with the ability to work collaboratively with researchers and other stakeholders.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As an MRA at ICON, you will support the design, execution, and management of clinical trials and research studies. You will play a crucial role in ensuring the accuracy and quality of data collection and analysis, contributing to the success of innovative treatments and therapies.
**Title:** Medical Research Associate (Phlebotomist/CMA/CNA)
**Job Type** : Full Time/Permanent
**Shift/Schedule:** Friday-Sunday Day Shift
**Location** : 100% on site San Antonio TX
**What You Will Be Doing:**
+ Assisting in the planning and execution of clinical trials and research studies, including data collection and management.
+ Supporting the research team with literature reviews, data entry, and analysis to inform study protocols and findings.
+ Maintaining accurate and organized research documentation, ensuring compliance with regulatory and ethical standards.
+ Collaborating with cross-functional teams to ensure timely completion of research tasks and adherence to study timelines.
+ Assisting with the preparation of research reports, manuscripts, and presentations for internal and external stakeholders.
**Your Profile:**
+ High School Diploma or equivalency with medical assistant training/certification or other allied health certification
+ Medical Assistant, Phlebotomy Technician, Paramedic, EMT, OR LVN preferably with two years of experience
+ Strong organizational and time management skills, with attention to detail in data collection and documentation.
+ Proficiency with research software and tools for data entry, analysis, and reporting.
+ Excellent communication and teamwork skills, with the ability to work collaboratively with researchers and other stakeholders.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
View Now
3
Medical Research Associate - PRN
66219 Lenexa, Kansas
ICON Clinical Research
Posted 2 days ago
Job Viewed
Job Description
Medical Research Associate (PRN) - On-Site - Lenexa, KS
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, Weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study.
**Title** : Medical Research Associate
**Location** : On-Site (Lenexa, KS)
**Job Type:** PRN hours currently available
**What You Will Be Doing:**
+ Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and Well-being throughout the research process.
+ You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures.
+ Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized.
+ Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort.
**Your Profile:**
+ A strong command of both English and the host country's language is essential, enabling effective communication and collaboration.
+ A High School Diploma or G.E.D. qualification
+ If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, We want to hear from you.
+ 1+ years of work experience in a medical or clinical field is preferred
+ If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage
+ Preferred Background: Paramedic/EMT, Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, Weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study.
**Title** : Medical Research Associate
**Location** : On-Site (Lenexa, KS)
**Job Type:** PRN hours currently available
**What You Will Be Doing:**
+ Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and Well-being throughout the research process.
+ You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures.
+ Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized.
+ Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort.
**Your Profile:**
+ A strong command of both English and the host country's language is essential, enabling effective communication and collaboration.
+ A High School Diploma or G.E.D. qualification
+ If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, We want to hear from you.
+ 1+ years of work experience in a medical or clinical field is preferred
+ If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage
+ Preferred Background: Paramedic/EMT, Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
View Now
4
Medical Research Associate - PRN
84190 Salt Lake City, Utah
ICON Clinical Research
Posted 13 days ago
Job Viewed
Job Description
Medical Research Associate - PRN - Clinical Research Trials - Salt Lake City, UT
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a **Medical Research Associate** to join our diverse and dynamic team. As a **Medical Research Associate** at **ICON** , you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study.
This **Medical Research Associate** is a **PRN** opportunity with flexible hours up to 30-hours per week, depending on candidate availability.
**What you will be doing**
+ Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process.
+ You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures.
+ Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized.
+ Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort.
**Your profile**
+ A strong command of both English and the host country's language is essential, enabling effective communication and collaboration.
+ A High School Diploma or G.E.D. qualification
+ If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you.
+ 1+ years of work experience in a medical or clinical field is preferred
+ If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage
+ Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a **Medical Research Associate** to join our diverse and dynamic team. As a **Medical Research Associate** at **ICON** , you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study.
This **Medical Research Associate** is a **PRN** opportunity with flexible hours up to 30-hours per week, depending on candidate availability.
**What you will be doing**
+ Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process.
+ You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures.
+ Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized.
+ Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort.
**Your profile**
+ A strong command of both English and the host country's language is essential, enabling effective communication and collaboration.
+ A High School Diploma or G.E.D. qualification
+ If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you.
+ 1+ years of work experience in a medical or clinical field is preferred
+ If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage
+ Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
View Now
5
Medical Research Associate - screening
84190 Salt Lake City, Utah
ICON Clinical Research
Posted 16 days ago
Job Viewed
Job Description
Medical Research Associate - Screening - Salt Lake City, UT
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study.
**What you will be doing**
+ Collect all assessments from study participants including obtaining consents and collecting medical history during every round.
+ Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process.
+ You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures.
+ Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized.
+ Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort.
**Your profile**
+ A strong command of both English and the host country's language is essential, enabling effective communication and collaboration.
+ A High School Diploma or G.E.D. qualification
+ If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you.
+ 1+ years of work experience in a medical or clinical field is preferred
+ If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage
+ Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study.
**What you will be doing**
+ Collect all assessments from study participants including obtaining consents and collecting medical history during every round.
+ Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process.
+ You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures.
+ Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized.
+ Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort.
**Your profile**
+ A strong command of both English and the host country's language is essential, enabling effective communication and collaboration.
+ A High School Diploma or G.E.D. qualification
+ If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you.
+ 1+ years of work experience in a medical or clinical field is preferred
+ If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage
+ Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
View Now
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6
Medical Research Associate (Full Time)
66219 Lenexa, Kansas
ICON Clinical Research
Posted 2 days ago
Job Viewed
Job Description
Medical Research Associate I (Full Time) - Lenexa, KS
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy eNugh to participate in the clinical trial according the protocol of a study.
**What you will be doing**
+ Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process.
+ You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures.
+ Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized.
+ Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort.
**Your profile**
+ A strong command of both English and the host country's language is essential, enabling effective communication and collaboration.
+ A High School Diploma or G.E.D. qualification
+ If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you.
+ 1+ years of work experience in a medical or clinical field is preferred
+ If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage
+ Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy eNugh to participate in the clinical trial according the protocol of a study.
**What you will be doing**
+ Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process.
+ You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures.
+ Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized.
+ Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort.
**Your profile**
+ A strong command of both English and the host country's language is essential, enabling effective communication and collaboration.
+ A High School Diploma or G.E.D. qualification
+ If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you.
+ 1+ years of work experience in a medical or clinical field is preferred
+ If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage
+ Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
View Now
7
Medical Research Associate (Medical Assistant/Phlebotomist)-
78284 San Antonio, Texas
ICON Clinical Research
Posted 1 day ago
Job Viewed
Job Description
Medical Research Associate (Medical Assistant/Phlebotomist)- ICON - Wed-Sun 1 PM-7AM- San Antonio TX
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As an MRA at ICON, you will support the design, execution, and management of clinical trials and research studies. You will play a crucial role in ensuring the accuracy and quality of data collection and analysis, contributing to the success of innovative treatments and therapies.
**Title:** Medical Research Associate (Phlebotomist/CMA/CNA)
**Job Type** : PRN/As Needed
**Shift/Schedule:** Wednesday-Sunday 1 PM-7 AM
**Location:** 100% on site San Antonio TX
**What You Will Be Doing:**
+ Assisting in the planning and execution of clinical trials and research studies, including data collection and management.
+ Supporting the research team with literature reviews, data entry, and analysis to inform study protocols and findings.
+ Maintaining accurate and organized research documentation, ensuring compliance with regulatory and ethical standards.
+ Collaborating with cross-functional teams to ensure timely completion of research tasks and adherence to study timelines.
+ Assisting with the preparation of research reports, manuscripts, and presentations for internal and external stakeholders.
**Your Profile:**
+ High School Diploma or equivalency with medical assistant training/certification or other allied health certification
+ Medical Assistant, Phlebotomy Technician, Paramedic, EMT, OR LVN preferably with two years of experience
+ Strong organizational and time management skills, with attention to detail in data collection and documentation.
+ Proficiency with research software and tools for data entry, analysis, and reporting.
+ Excellent communication and teamwork skills, with the ability to work collaboratively with researchers and other stakeholders.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As an MRA at ICON, you will support the design, execution, and management of clinical trials and research studies. You will play a crucial role in ensuring the accuracy and quality of data collection and analysis, contributing to the success of innovative treatments and therapies.
**Title:** Medical Research Associate (Phlebotomist/CMA/CNA)
**Job Type** : PRN/As Needed
**Shift/Schedule:** Wednesday-Sunday 1 PM-7 AM
**Location:** 100% on site San Antonio TX
**What You Will Be Doing:**
+ Assisting in the planning and execution of clinical trials and research studies, including data collection and management.
+ Supporting the research team with literature reviews, data entry, and analysis to inform study protocols and findings.
+ Maintaining accurate and organized research documentation, ensuring compliance with regulatory and ethical standards.
+ Collaborating with cross-functional teams to ensure timely completion of research tasks and adherence to study timelines.
+ Assisting with the preparation of research reports, manuscripts, and presentations for internal and external stakeholders.
**Your Profile:**
+ High School Diploma or equivalency with medical assistant training/certification or other allied health certification
+ Medical Assistant, Phlebotomy Technician, Paramedic, EMT, OR LVN preferably with two years of experience
+ Strong organizational and time management skills, with attention to detail in data collection and documentation.
+ Proficiency with research software and tools for data entry, analysis, and reporting.
+ Excellent communication and teamwork skills, with the ability to work collaboratively with researchers and other stakeholders.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
View Now
8
Medical Affairs Research Associate
92604 Woodbridge, California
Kelly Services
Posted 2 days ago
Job Viewed
Job Description
**Medical Affairs Research Associate**
**Hybrid - Onsite in Irvine, CA Tuesday/Thursday and every other Friday**
**Weekends, Domestic travel will be required up to 40%, occasional weekends**
**Essential Duties & Responsibilities:**
+ Independently works on in-vivo and bench models for the investigation of cardiac products and how they perform in a simulated clinical use setting.
+ Independently identifies data outliers, prepares data for statistical analysis for in-vivo study data
+ Assists in in-vivo protocol execution, may develop or be a part of developing new processes/test fixtures or methods for medical device testing
+ Interfaces with internal customers within R&D, Medical Safety, and Quality
+ May be asked to assist in model development for proper statistical analysis of in-vivo, clinical, and other parametric datasets
+ May be asked to assist in the production of mathematical and/or computational modeling of cardiac systems using electromechanical design and controls
+ Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance as well as develop a strong working knowledge of design controls and quality assurance standards of procedure.
+ Has a working knowledge of good laboratory practices and operating room procedures
+ Willingness to develop an understanding of cardiac electrophysiology procedures and the products used
+ Excellent oral and written communication skills are required
**Qualification Requirements:**
+ Experience in working with soft tissue (handling, histology and fixation, including staining and dissection). Previous experience with Bioinstrumentation laboratory equipment.
+ Experience in working with **large animal** (porcine/ovine, etc) and bench top models.
+ Strong working knowledge with all of the programs listed: MicroSoft office (specifically Excel and PowerPoint), statistical analysis tools (such as SAS or Minitab, R, SPSS), and working knowledge of Mathematical modeling MatLab software or Prism Job Description
**Education & Experience:**
+ A minimum MS in the Sciences or Engineering or equivalent from an accredited Laboratory Science program, College or University.
+ At least 5-8 years of Laboratory experience (Industry and/or Hospital); and/or related medical device development experience and/or training is required. Experience in cardiology, cardiac biophysics and anatomy are preferred
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.
**Hybrid - Onsite in Irvine, CA Tuesday/Thursday and every other Friday**
**Weekends, Domestic travel will be required up to 40%, occasional weekends**
**Essential Duties & Responsibilities:**
+ Independently works on in-vivo and bench models for the investigation of cardiac products and how they perform in a simulated clinical use setting.
+ Independently identifies data outliers, prepares data for statistical analysis for in-vivo study data
+ Assists in in-vivo protocol execution, may develop or be a part of developing new processes/test fixtures or methods for medical device testing
+ Interfaces with internal customers within R&D, Medical Safety, and Quality
+ May be asked to assist in model development for proper statistical analysis of in-vivo, clinical, and other parametric datasets
+ May be asked to assist in the production of mathematical and/or computational modeling of cardiac systems using electromechanical design and controls
+ Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance as well as develop a strong working knowledge of design controls and quality assurance standards of procedure.
+ Has a working knowledge of good laboratory practices and operating room procedures
+ Willingness to develop an understanding of cardiac electrophysiology procedures and the products used
+ Excellent oral and written communication skills are required
**Qualification Requirements:**
+ Experience in working with soft tissue (handling, histology and fixation, including staining and dissection). Previous experience with Bioinstrumentation laboratory equipment.
+ Experience in working with **large animal** (porcine/ovine, etc) and bench top models.
+ Strong working knowledge with all of the programs listed: MicroSoft office (specifically Excel and PowerPoint), statistical analysis tools (such as SAS or Minitab, R, SPSS), and working knowledge of Mathematical modeling MatLab software or Prism Job Description
**Education & Experience:**
+ A minimum MS in the Sciences or Engineering or equivalent from an accredited Laboratory Science program, College or University.
+ At least 5-8 years of Laboratory experience (Industry and/or Hospital); and/or related medical device development experience and/or training is required. Experience in cardiology, cardiac biophysics and anatomy are preferred
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.
View Now
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