10,619 Healthcare Research jobs in the United States
Associate General Counsel, Healthcare & Research - #Staff

Posted 1 day ago
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Job Description
Working with the practice group leader and other OGC colleagues, the AGC will share responsibility for providing legal counsel across the research and academic medical center enterprise, including both transactional and regulatory compliance support. The AGC will also be responsible for legal issues related to graduate medical education conducted through the School of Medicine and Bloomberg School of Public Health.
The successful candidate will have the relevant years of legal experience counseling on legal issues surrounding academic research, an understanding of the regulatory requirements associated with the responsible conduct of research, particularly federally funded research, and a strong proficiency in drafting and negotiating complex transactional agreements, including for research purposes.
OGC is seeking an attorney who is sensitive to and understands the special nature of working in an academic institution where the need for a collaborative working style, flexibility, adaptability, and patience are critical to success. A lawyer who sees the big picture, is practical, and who will bring to the position a strong work ethic, energy, a sense of urgency and a passion for the mission of JHU.
**Specific Duties and Responsibilities**
+ Provide legal guidance and support regarding compliance with applicable policies, procedures, laws, and regulations related to JHU's research activities, both domestically and internationally.
+ Work with clients and colleagues on a broad range of issues related to sponsored research, including advising on animal and human subjects research, intellectual property, privacy, conflict of interest, award compliance, research integrity, investigational drugs and devices, clinical trials, and other regulatory requirements.
+ Support the research administration offices in their negotiation and administration of sponsored research (both basic laboratory and clinical trial research) and drafting of relevant communications with government agencies, universities, foundations, and biotech and pharmaceutical companies related thereto, including sponsored research agreements, data use agreements, material transfer agreements, and confidentiality agreements.
+ Provide legal advice on research misconduct proceedings and review of inquiry and investigation reports for legal sufficiency.
+ Interpret, draft, and revise relevant policies and procedures and work with the Compliance office to support research compliance matters.
+ Serve on relevant JHU committees and provide legal counsel on committee work.
+ Other areas and projects as assigned.
**Minimum Qualifications**
+ Juris Doctor ("JD") Degree from an ABA accredited nationally recognized law school with superior academic credentials.
+ Active membership in good standing in at least one state bar association. Satisfaction of all applicable requirements for attorneys practicing in the State of Maryland.
+ Five plus years of relevant experience providing advice and counsel on transactional and regulatory compliance matters within: (i) a college, university, or academic medical center legal department; (ii) a law firm working for large, complex clients; (iii) a relevant nonprofit institution; or (iv) a relevant federal government department or agency.
+ Additional education may substitute for required experience and additional related experience may substitute for required education beyond HS Diploma/Graduation Equivalent, to the extent permitted by the JHU equivalency formula.
**Preferred Qualifications**
+ Experience counseling on complex legal issues and demonstrated ability to address compliance with the full range of applicable laws, regulations, rules, and policies that affect JHU's activities in healthcare and research.
+ Expertise drafting and negotiating complex contracts (e.g., sponsored research agreements, confidentiality agreements, clinical trial agreements, data use agreements, licensing and other intellectual property agreements, material transfer agreements, memorandum of understanding, affiliation agreements, professional service agreements)
+ Willingness to learn new subject areas and ability to implement newly acquired knowledge.
+ Commitment to providing excellent customer service through prompt and practical legal advice.
+ Strong analytic skills, with an ability to identify and apply sound judgment and reasoning.
+ Ability to work effectively, both independently and as part of a team, in a fast-paced environment, to handle multiple complex tasks, and to prioritize competing deadlines generated by multiple constituencies.
+ Ability to communicate clearly, concisely, and collegially with JHU personnel at all levels of education, skill, and responsibility, as well as with external sponsors and outside counsel.
+ Ability to maintain confidentiality and exercise discretion and tact when handling sensitive issues.
+ Appropriate self-awareness, including when to escalate matters.
+ Experience practicing in a higher education or academic medical setting strongly preferred.
Classified Title: Associate General Counsel
Job Posting Title (Working Title): Associate General Counsel, Healthcare & Research
Role/Level/Range: ATP/04/PI
Starting Salary Range: $135,900 - $238,400 Annually (Commensurate w/exp.)
Employee group: Full Time
Schedule: Monday-Friday, 8:30-5pm
FLSA Status: Exempt
Location: Hybrid/School of Medicine Campus
Department name: VP and General Counsel Office of
Personnel area: University Administration
The listed salary range represents the minimum and maximum Johns Hopkins University offers for this position, based on a good faith estimate at the time of posting. Actual compensation will vary depending on factors such as location, skills, experience, market conditions, education, and internal equity. Not all candidates will qualify for the highest salary in the range.
Johns Hopkins provides a comprehensive benefits package supporting health, career, and retirement. Learn more: Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
EEO is the Law
Associate General Counsel, Healthcare & Research/Transactions - #Staff

Posted 1 day ago
Job Viewed
Job Description
**Specific Duties and Responsibilities**
+ Serve as lead transactional attorney on behalf of JHU in negotiating, structuring, and managing joint JHU/JHHS affiliations with, and acquisitions of, third party entities including health systems, FQHCs, physician practices and community hospitals.
+ Spot regulatory issues and, in partnership with other internal and external counsel as needed, ensure compliance with the Stark Act and antikickback laws.
+ Keep abreast of industry trends and regulatory developments affecting healthcare providers.
+ Advise on creating new service lines, new quality metrics programs and establishing new modes of healthcare service delivery (including telehealth, concierge, and related modalities).
+ Assist in the documentation of agreements within a growing academic medical center, including agreements among the components of that academic medical center.
+ Advise on healthcare and billing compliance, in partnership with the Chief Compliance Officer, telemedicine matters, and on faculty/physician compensation.
+ Provide guidance and assistance to other colleagues in the University's Office of the Senior Vice President and General Counsel in a highly collaborative fashion.
**Minimum Qualifications**
+ A Juris Doctor Degree from an accredited law school.
+ Active membership in good standing in at least one state bar association. Satisfaction of all applicable requirements for attorneys practicing in-house in the State of Maryland.
+ Eight or more (8+) years of legal experience, including a minimum of five years (5+) spent advising health care clients, preferably academic medical centers, or similar complex health care organizations.
+ Experience drafting documents of substantial complexity in a high-volume environment, including acquisition documents for physician practices, and negotiating professional services, employment, and other agreements involving physicians and physician groups.
+ Subject matter expertise involving healthcare regulatory issues that arise in the context of transactions.
+ Additional education may substitute for required experience and additional related experience may substitute for required education beyond HS Diploma/Graduation Equivalent, to the extent permitted by the JHU equivalency formula.
**Preferred Qualifications**
+ Extensive knowledge in the areas of healthcare service contracts, physician compensation and employment law, and related transaction is preferred.
+ Experience in emerging models of compensation in health care and compliance with CMS regulations and related laws is desired.
+ Strong relationship building skills and ability to work collaboratively and be a highly supportive member of multiple legal/client teams.
+ Ability to communicate verbally and in writing, with all levels of university and Johns Hopkins School of Medicine, physicians, patients, visitors, and attorneys.
+ Track record of maintaining positive, collaborative, and effective relationships with physicians, peers, subordinates, and superiors.
+ Excellent legal analytical skills.
+ Able to manage a high volume of work and multiple priorities in a fast-paced environment.
+ A counselor, mediator, and problem solver.
+ A team player with superior listening skills.
+ Integrity of the highest order.
Classified Title: Associate General Counsel
Job Posting Title (Working Title): Associate General Counsel, Healthcare & Research/Transactions
Role/Level/Range: ATP/04/PI
Starting Salary Range: $135,900 - $238,400 Annually (Commensurate w/exp.)
Employee group: Full Time
Schedule: Monday-Friday, 8:30-5pm
FLSA Status: Exempt
Location: Hybrid/School of Medicine Campus
Department name: VP and General Counsel Office of
Personnel area: University Administration
The listed salary range represents the minimum and maximum Johns Hopkins University offers for this position, based on a good faith estimate at the time of posting. Actual compensation will vary depending on factors such as location, skills, experience, market conditions, education, and internal equity. Not all candidates will qualify for the highest salary in the range.
Johns Hopkins provides a comprehensive benefits package supporting health, career, and retirement. Learn more: Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
EEO is the Law
Medical Research Associate
Posted 7 days ago
Job Viewed
Job Description
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
Medical Research Associate

Posted 15 days ago
Job Viewed
Job Description
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
Medical Research Associate - PRN

Posted 1 day ago
Job Viewed
Job Description
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
Medical Research Associate - PRN
Posted 12 days ago
Job Viewed
Job Description
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
Medical Research Associate - screening

Posted 15 days ago
Job Viewed
Job Description
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
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Clinical Research Associate
Posted today
Job Viewed
Job Description
Job Title : Clinical Research Associate
Location: Los Angeles, CA 90025
Start Date: 11/03/2025
Duration: 13 weeks
Schedule Shift: Day 5x8-Hour (08:00 - 17:00)
Pay Rate: $33/hr. Gross weekly : $1320
Description :
Position Summary:
This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace.
Requirements:
- High School Diploma/GED required. Bachelor's degree preferred.
- 1 year Clinical research related experience required.
- Chemo, Oncology, or pharmaceutical research experience
Clinical Research Associate
Posted today
Job Viewed
Job Description
HungaroTrial is the largest regional CRO in Central and Eastern Europe with 10 offices in the region and USA, plus Business Development office in London, UK. Due to the expansion of our operations in the USA we are looking for CRA colleagues with at least 2 years of active monitoring experience.
As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical studies in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures, ICH-GCP guidelines and the applicable regulations and SOPs.
Main duties and responsibilities
- Initiate, monitor and close-out clinical studies on study sites in accordance with applicable regulations, guidelines of ICH-GCP and standard operation procedures;
- Prepare and perform regulatory and ethics submission (drug, medical device, non-interventional) for approval in accordance with applicable regulations, guidelines of ICH GCP and standard operation procedures of HungaroTrial (e.g. able to perform initial CA and EC submissions, amendment, notification, progress and safety report submissions, contract negotiations without direct supervision);
- Supportcontracting procedure between Sponsor and Investigational sites;
- Perform feasibilities and pre-study evaluations ;
- Document activity in accordance with ICH-GCP and standard operation procedures of HungaroTrial;
- Prepare a summary (report) of activities as requested by the Manager.
Requirements
- Bachelor degree in life sciences
- at least 2 years experience in CRA role
- experience in Oncology clinical trials
- native level of English
- Confident IT skills
- Driver’s license
- effective communication, customer focus, teamwork, time management, motivation to learn and develop
What we can offer
- Attractive and competitive salary
- Dedicated and supportive team
- Multinational environment
- Regular team buildings and company events
We take special attention to the balance of the work and your private life.
Clinical Research Associate
Posted today
Job Viewed
Job Description
Responsible for pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and management, adverse event management to ensure protoco Clinical Research, Research Associate, Clinical, Associate, Research, Healthcare, Education