653 Fieldwork jobs in the United States
Fieldwork Trainee
Gastonia, North Carolina
hopebridge
Posted today
Job Viewed
Job Description
Job Description
Job Description
As a Fieldwork Trainee, you’ll be a key player on our therapy dream team, working under the direct supervision of a Board Certified Behavior Analyst (BCBA). You’ll split your time between providing 1:1 therapy for amazing young learners and diving into the world of clinical assessments, data analysis, and program development to support you in your path toward your BCBA credential.
Pay Rate: $23-$5/hour with RBT certification
Fieldwork Trainee Benefits :
- $125 P ofessional Development Stipend : Invest in your growth and expertise in Autism intervention
- An opportunity to earn restricted and unrestricted supervision hours
- Exclusive Access to Robust Learning Opportunities (mentorship, HBx seminars, journal clubs, study sessions, Funds for Fellows, and more!)
- Paid exam application and scheduling fees
- Free access to exam study materials (e.g., workshops and mock exams)
- Exam pass bonus
- Health, Vision, and Dental Insurance: Prioritize your physical well-being
- Wellness Programs: Nurture a healthy work-life balance
- 19 Days of PTO : Enjoy paid time off, holidays, and a flex holiday
- 401K Retirement Options with Company Match: Secure your financial future
- Rain Flexible Pay benefits available
- Opportunity to Relocate : Explore exciting career possibilities in any of our states
- Deliver 1:1 ABA therapy to children, helping them learn and grow every single day!
- Collaborate with the BCBA to analyze data, review treatment plans, and make magic happen.
- Lead training for our awesome team of RBTs and help them be the best they can be.
- Collaborate with a diverse team of specialists in a multidisciplinary therapy environment to provide well-rounded care.
- Participate in assessments, report writing, parent consultations, and more!
- Stay on top of the latest ABA trends and techniques – because we love to learn and grow just as much as we love helping!
- You’re currently enrolled in or have completed a Master’s program leading to BCBA certification.
- You’ve got 1750+ documented fieldwork supervision hours (or are well on your way) and are balancing your time between restricted/unrestricted hours like a pro.
- Anticipation of sitting for the BCBA exam within 4 mos.
- A passion for ABA, with the skills to back it up (knowledge of ABA methodology is a must).
- A positive attitude, a desire to learn, and the ability to rock some serious time management.
- Ethical, professional, and ready to make a meaningful impact – always with a smile!
- You’ll be part of a supportive, dynamic team that’s dedicated to your growth.
- Get hands-on experience working with a variety of clients and expand your skill set.
- Access to ongoing professional development and the latest in ABA training.
- A chance to work in a fun, fast-paced environment where your hard work makes a difference every day.
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0
Fieldwork Trainee
Savannah, Tennessee
hopebridge
Posted today
Job Viewed
Job Description
Job Description
Job Description
As a Fieldwork Trainee, you’ll be a key player on our therapy dream team, working under the direct supervision of a Board Certified Behavior Analyst (BCBA). You’ll split your time between providing 1:1 therapy for amazing young learners and diving into the world of clinical assessments, data analysis, and program development to support you in your path toward your BCBA credential.
Pay Rate: $23-$5/hour with RBT certification
Fieldwork Trainee Benefits :
- $125 P ofessional Development Stipend : Invest in your growth and expertise in Autism intervention
- An opportunity to earn restricted and unrestricted supervision hours
- Exclusive Access to Robust Learning Opportunities (mentorship, HBx seminars, journal clubs, study sessions, Funds for Fellows, and more!)
- Paid exam application and scheduling fees
- Free access to exam study materials (e.g., workshops and mock exams)
- Exam pass bonus
- Health, Vision, and Dental Insurance: Prioritize your physical well-being
- Wellness Programs: Nurture a healthy work-life balance
- 18 Days of PTO : Enjoy paid time off, holidays, and a flex holiday
- 401K Retirement Options with Company Match: Secure your financial future
- Rain Flexible Pay benefits available
- Opportunity to Relocate : Explore exciting career possibilities in any of our states
- Deliver 1:1 ABA therapy to children, helping them learn and grow every single day!
- Collaborate with the BCBA to analyze data, review treatment plans, and make magic happen.
- Lead training for our awesome team of RBTs and help them be the best they can be.
- Collaborate with a diverse team of specialists in a multidisciplinary therapy environment to provide well-rounded care.
- Participate in assessments, report writing, parent consultations, and more!
- Stay on top of the latest ABA trends and techniques – because we love to learn and grow just as much as we love helping!
- You’re currently enrolled in or have completed a Master’s program leading to BCBA certification.
- You’ve got 1750+ documented fieldwork supervision hours (or are well on your way) and are balancing your time between restricted/unrestricted hours like a pro.
- Anticipation of sitting for the BCBA exam within 4 mos.
- A passion for ABA, with the skills to back it up (knowledge of ABA methodology is a must).
- A positive attitude, a desire to learn, and the ability to rock some serious time management.
- Ethical, professional, and ready to make a meaningful impact – always with a smile!
- You’ll be part of a supportive, dynamic team that’s dedicated to your growth.
- Get hands-on experience working with a variety of clients and expand your skill set.
- Access to ongoing professional development and the latest in ABA training.
- A chance to work in a fun, fast-paced environment where your hard work makes a difference every day.
View Now
1
Fieldwork Placement Application*
48567 Flint, Michigan
Mid-Michigan Area Public Schools Consortium
Posted 22 days ago
Job Viewed
Job Description
Position Type:
Student Placements
Date Posted:
3/20/2024
District:
Genesee Intermediate School District PLEASE BE ADVISED THIS IS NOT A POSTING, THIS JOB ID IS FOR FIELDWORK STUDENT APPLICATION SUBMISSIONS FOR COLLEGE/UNIVERSITY REQUIREMENT. STUDENTS SUBMITTING AN APPLICATION SHOULD VERIFY THERE IS AN ESTABLISHED AFFILATION AGREEMENT WITH THEIR COLLEGE/UNIVERSITY.
Thank you for your interest in becoming a fieldwork student at Genesee Intermediate School District for your program requirement.
Please begin by familiarizing yourself with Voluntary Internship Program Administrative Guideline (3120.06A) as it details the internship expectations.
Application Procedure:
Individuals wishing to serve as a fieldwork students with the district will submit an application to the Human Resources and Operations Department, at least thirty (30) days prior to the requested start date.
Pre-Fieldwork Experience:
I. Complete an Application Online
On the application you will be asked to attach your transcripts, resume, TB, and specify your goals and objectives for your program requirement. Please insure to complete all the required fields and attach the requested documents to prevent your application from displaying incomplete.
II. Interview with a Human Resources Representative
Upon completion of your application, please contact human resources at ( to set-up an interview.
III. Complete Fieldwork Student Fingerprinting (You will be scheduled on the day of your interview)
Cost of $52.00 check and/or money order.
IV. Orientation/Interview with Supervising Mentor/Program Administrator (Upon district program request)
V. Complete District Mandatory Trainings (You will receive a separate e-mail from SafeSchools)
Post Fieldwork Experience:
I. Exit Interview with Human Resources
Please call to make your appointment two weeks prior to your last day of your internship.
Should you have an questions, please feel free to contact Human Resources at ( .
Attachment(s):
Student Placements
Date Posted:
3/20/2024
District:
Genesee Intermediate School District PLEASE BE ADVISED THIS IS NOT A POSTING, THIS JOB ID IS FOR FIELDWORK STUDENT APPLICATION SUBMISSIONS FOR COLLEGE/UNIVERSITY REQUIREMENT. STUDENTS SUBMITTING AN APPLICATION SHOULD VERIFY THERE IS AN ESTABLISHED AFFILATION AGREEMENT WITH THEIR COLLEGE/UNIVERSITY.
Thank you for your interest in becoming a fieldwork student at Genesee Intermediate School District for your program requirement.
Please begin by familiarizing yourself with Voluntary Internship Program Administrative Guideline (3120.06A) as it details the internship expectations.
Application Procedure:
Individuals wishing to serve as a fieldwork students with the district will submit an application to the Human Resources and Operations Department, at least thirty (30) days prior to the requested start date.
Pre-Fieldwork Experience:
I. Complete an Application Online
On the application you will be asked to attach your transcripts, resume, TB, and specify your goals and objectives for your program requirement. Please insure to complete all the required fields and attach the requested documents to prevent your application from displaying incomplete.
II. Interview with a Human Resources Representative
Upon completion of your application, please contact human resources at ( to set-up an interview.
III. Complete Fieldwork Student Fingerprinting (You will be scheduled on the day of your interview)
Cost of $52.00 check and/or money order.
IV. Orientation/Interview with Supervising Mentor/Program Administrator (Upon district program request)
V. Complete District Mandatory Trainings (You will receive a separate e-mail from SafeSchools)
Post Fieldwork Experience:
I. Exit Interview with Human Resources
Please call to make your appointment two weeks prior to your last day of your internship.
Should you have an questions, please feel free to contact Human Resources at ( .
Attachment(s):
- ag3120.06 Voluntary Internship Program.pdf
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2
Clinical Coordinator- OTA (Academic Fieldwork Coordinator)
32318 Crawfordville, Florida
Keiser University
Posted 21 days ago
Job Viewed
Job Description
The Clinical Coordinator position plans, coordinates, facilitates, administers, and monitors, activities on behalf of the academic program and in coordination with academic and clinical faculty. These activities ensure the quality of our students learning experience during clinical education. Clinical Coordinators accomplish this through:
- Assists with the development and assessment of the clinical education component of the curriculum with the Program Director.
- Coordination and implementation of the clinical education component of the curriculum including site placements, site visits, and evaluation.
- Responsible for facilitating students' clinical education.
- Responsible for ensuring clinical education program compliance.
- Minimum of a bachelor's degree (A.S. degree in OTA is preferred). A bachelor's degree can by in any field.
- At least 2 years of clinical practice experience as an occupational therapist or occupational therapy assistant (2018 ACOTE Standards).
- Current, unrestricted Florida licensed occupational therapist or occupational therapy assistant.
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3
Clinical Coordinator- MSOT (Academic Fieldwork Coordinator)
33222 Miami, Florida
Keiser University
Posted 21 days ago
Job Viewed
Job Description
The Clinical Coordinator position plans, coordinates, facilitates, administers, and monitors, activities on behalf of the academic program and in coordination with academic and clinical faculty. These activities ensure the quality of our students learning experience during clinical education. Clinical Coordinators accomplish this through:
- Assists with the development and assessment of the clinical education component of the curriculum with the Program Director
- Coordination and implementation of the clinical education component of the curriculum including site placements, site visits, and evaluation
- Responsible for facilitating students' clinical education
- Responsible for ensuring clinical education program compliance
- Ensuring that the fieldwork experience reflects the sequence and scope of content in the curriculum design
- Be an occupational therapist who is licensed or otherwise regulated according to regulations in the state(s) or jurisdiction(s) in which the program is located (2023 ACOTE Standards).
- Hold a minimum of a master's degree or PhD awarded by an institution that is accredited by a USDE-recognized institutional accrediting agency (2023 ACOTE Standards).
- Have at least 2 years of documented experience in the field of occupational therapy, which must include clinical practice experience as an occupational therapist and professional experience as a fieldwork educator or documentation of training in the roles and responsibilities of a fieldwork educator (2023 ACOTE Standards).
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4
Site Research Assistant - Hammond, LA
70434 Covington, Louisiana
IQVIA
Posted today
Job Viewed
Job Description
**Job Title:** Research Assistant
**Work Set-Up:** Working On-site
**Scheduled Weekly Hours:** 24 Hours
**Job Profile Summary:** This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.
**Responsibilities:**
+ EDC Entry and Query Resolution
+ Develop strong working relationships and maintain effective communication with study team members.
+ Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
+ Assist with the screening, recruiting, and enrollment of research subjects.
+ Perform patient/research participant scheduling.
+ Collect patient/research participant history.
+ Coordinate follow-up care and laboratory procedures.
+ Adhere to an IRB-approved protocol.
+ Assist in the informed consent process of research subjects.
+ Support the safety of research subjects.
+ Coordinate protocol-related research procedures, study visits, and follow-up care.
+ Comply with company and Sponsor policies, standard operating procedures (SOPs), and guidelines.
+ Schedule subject visits and procedures.
**Qualifications:**
+ Equivalent education and experience - High School Diploma and 1 years' relevant work experience in clinical research.
+ At least 1 year experience working in a clinical research setting preferred.
+ Working knowledge of clinical trials.
+ Working knowledge of the principles of Good Clinical Practices (GCP).
+ In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
+ Skill in carrying out required clinical procedures.
+ Working knowledge of medical terminology.
+ Ability to pay close attention to detail.
+ Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
+ Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
_Please note, this position is not eligible for sponsorship._
#LI-CES and #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Work Set-Up:** Working On-site
**Scheduled Weekly Hours:** 24 Hours
**Job Profile Summary:** This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.
**Responsibilities:**
+ EDC Entry and Query Resolution
+ Develop strong working relationships and maintain effective communication with study team members.
+ Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
+ Assist with the screening, recruiting, and enrollment of research subjects.
+ Perform patient/research participant scheduling.
+ Collect patient/research participant history.
+ Coordinate follow-up care and laboratory procedures.
+ Adhere to an IRB-approved protocol.
+ Assist in the informed consent process of research subjects.
+ Support the safety of research subjects.
+ Coordinate protocol-related research procedures, study visits, and follow-up care.
+ Comply with company and Sponsor policies, standard operating procedures (SOPs), and guidelines.
+ Schedule subject visits and procedures.
**Qualifications:**
+ Equivalent education and experience - High School Diploma and 1 years' relevant work experience in clinical research.
+ At least 1 year experience working in a clinical research setting preferred.
+ Working knowledge of clinical trials.
+ Working knowledge of the principles of Good Clinical Practices (GCP).
+ In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
+ Skill in carrying out required clinical procedures.
+ Working knowledge of medical terminology.
+ Ability to pay close attention to detail.
+ Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
+ Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
_Please note, this position is not eligible for sponsorship._
#LI-CES and #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
View Now
5
Site Research Assistant - Kenosha, WI
53140 Kenosha, Wisconsin
IQVIA
Posted 4 days ago
Job Viewed
Job Description
**Job Title:** Research Assistant
**Work Set-Up:** Working On-site
**Scheduled Weekly Hours:** 24 Hours
**Job Profile Summary:** This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.
**Responsibilities:**
+ EDC Entry and Query Resolution
+ Develop strong working relationships and maintain effective communication with study team members.
+ Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
+ Assist with the screening, recruiting, and enrollment of research subjects.
+ Perform patient/research participant scheduling.
+ Collect patient/research participant history.
+ Coordinate follow-up care and laboratory procedures.
+ Adhere to an IRB-approved protocol.
+ Assist in the informed consent process of research subjects.
+ Support the safety of research subjects.
+ Coordinate protocol-related research procedures, study visits, and follow-up care.
+ Comply with company and Sponsor policies, standard operating procedures (SOPs), and guidelines.
+ Schedule subject visits and procedures.
**Qualifications:**
+ Equivalent education and experience - High School Diploma and 1 years' relevant work experience in clinical research.
+ At least 1 year experience working in a clinical research setting preferred.
+ Working knowledge of clinical trials.
+ Working knowledge of the principles of Good Clinical Practices (GCP).
+ In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
+ Skill in carrying out required clinical procedures.
+ Working knowledge of medical terminology.
+ Ability to pay close attention to detail.
+ Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
+ Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
_Please note, this position is not eligible for sponsorship._
#LI-CES and #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Work Set-Up:** Working On-site
**Scheduled Weekly Hours:** 24 Hours
**Job Profile Summary:** This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.
**Responsibilities:**
+ EDC Entry and Query Resolution
+ Develop strong working relationships and maintain effective communication with study team members.
+ Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
+ Assist with the screening, recruiting, and enrollment of research subjects.
+ Perform patient/research participant scheduling.
+ Collect patient/research participant history.
+ Coordinate follow-up care and laboratory procedures.
+ Adhere to an IRB-approved protocol.
+ Assist in the informed consent process of research subjects.
+ Support the safety of research subjects.
+ Coordinate protocol-related research procedures, study visits, and follow-up care.
+ Comply with company and Sponsor policies, standard operating procedures (SOPs), and guidelines.
+ Schedule subject visits and procedures.
**Qualifications:**
+ Equivalent education and experience - High School Diploma and 1 years' relevant work experience in clinical research.
+ At least 1 year experience working in a clinical research setting preferred.
+ Working knowledge of clinical trials.
+ Working knowledge of the principles of Good Clinical Practices (GCP).
+ In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
+ Skill in carrying out required clinical procedures.
+ Working knowledge of medical terminology.
+ Ability to pay close attention to detail.
+ Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
+ Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
_Please note, this position is not eligible for sponsorship._
#LI-CES and #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
View Now
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6
Site Research Assistant - Hallandale Beach, FL
33180 Aventura, Florida
IQVIA
Posted today
Job Viewed
Job Description
**Job Title:** Research Assistant
**Work Set-Up:** Working On-site
**Scheduled Weekly Hours:** 24 Hours
**Job Profile Summary:** This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.
**Responsibilities:**
+ EDC Entry and Query Resolution
+ Develop strong working relationships and maintain effective communication with study team members.
+ Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
+ Assist with the screening, recruiting, and enrollment of research subjects.
+ Perform patient/research participant scheduling.
+ Collect patient/research participant history.
+ Coordinate follow-up care and laboratory procedures.
+ Adhere to an IRB-approved protocol.
+ Assist in the informed consent process of research subjects.
+ Support the safety of research subjects.
+ Coordinate protocol-related research procedures, study visits, and follow-up care.
+ Comply with company and Sponsor policies, standard operating procedures (SOPs), and guidelines.
+ Schedule subject visits and procedures.
**Qualifications:**
+ Equivalent education and experience: a minimum of an associate's degree.
+ At least 1 year experience working in a clinical research setting preferred.
+ Working knowledge of clinical trials.
+ Working knowledge of the principles of Good Clinical Practices (GCP).
+ In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
+ Skill in carrying out required clinical procedures.
+ Working knowledge of medical terminology.
+ Ability to pay close attention to detail.
+ Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
+ Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
_Please note, this position is not eligible for sponsorship._
#LI-CES and #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Work Set-Up:** Working On-site
**Scheduled Weekly Hours:** 24 Hours
**Job Profile Summary:** This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.
**Responsibilities:**
+ EDC Entry and Query Resolution
+ Develop strong working relationships and maintain effective communication with study team members.
+ Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
+ Assist with the screening, recruiting, and enrollment of research subjects.
+ Perform patient/research participant scheduling.
+ Collect patient/research participant history.
+ Coordinate follow-up care and laboratory procedures.
+ Adhere to an IRB-approved protocol.
+ Assist in the informed consent process of research subjects.
+ Support the safety of research subjects.
+ Coordinate protocol-related research procedures, study visits, and follow-up care.
+ Comply with company and Sponsor policies, standard operating procedures (SOPs), and guidelines.
+ Schedule subject visits and procedures.
**Qualifications:**
+ Equivalent education and experience: a minimum of an associate's degree.
+ At least 1 year experience working in a clinical research setting preferred.
+ Working knowledge of clinical trials.
+ Working knowledge of the principles of Good Clinical Practices (GCP).
+ In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
+ Skill in carrying out required clinical procedures.
+ Working knowledge of medical terminology.
+ Ability to pay close attention to detail.
+ Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
+ Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
_Please note, this position is not eligible for sponsorship._
#LI-CES and #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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7
Site Research Assistant -Johns Creek, GA
30309 Midtown Atlanta, Georgia
IQVIA
Posted today
Job Viewed
Job Description
**Job Title:** Research Assistant
**Work Set-Up:** Working On-site
**Scheduled Weekly Hours:** 24 Hours
**Job Profile Summary:** This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.
**Responsibilities:**
+ EDC Entry and Query Resolution
+ Develop strong working relationships and maintain effective communication with study team members.
+ Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
+ Assist with the screening, recruiting, and enrollment of research subjects.
+ Perform patient/research participant scheduling.
+ Collect patient/research participant history.
+ Coordinate follow-up care and laboratory procedures.
+ Adhere to an IRB-approved protocol.
+ Assist in the informed consent process of research subjects.
+ Support the safety of research subjects.
+ Coordinate protocol-related research procedures, study visits, and follow-up care.
+ Comply with company and Sponsor policies, standard operating procedures (SOPs), and guidelines.
+ Schedule subject visits and procedures.
**Qualifications:**
+ Equivalent education and experience - High School Diploma and 1 years' relevant work experience in clinical research.
+ At least 1 year experience working in a clinical research setting preferred.
+ Working knowledge of clinical trials.
+ Working knowledge of the principles of Good Clinical Practices (GCP).
+ In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
+ Skill in carrying out required clinical procedures.
+ Working knowledge of medical terminology.
+ Ability to pay close attention to detail.
+ Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
+ Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
_Please note, this position is not eligible for sponsorship._
#LI-CES and #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Work Set-Up:** Working On-site
**Scheduled Weekly Hours:** 24 Hours
**Job Profile Summary:** This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.
**Responsibilities:**
+ EDC Entry and Query Resolution
+ Develop strong working relationships and maintain effective communication with study team members.
+ Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
+ Assist with the screening, recruiting, and enrollment of research subjects.
+ Perform patient/research participant scheduling.
+ Collect patient/research participant history.
+ Coordinate follow-up care and laboratory procedures.
+ Adhere to an IRB-approved protocol.
+ Assist in the informed consent process of research subjects.
+ Support the safety of research subjects.
+ Coordinate protocol-related research procedures, study visits, and follow-up care.
+ Comply with company and Sponsor policies, standard operating procedures (SOPs), and guidelines.
+ Schedule subject visits and procedures.
**Qualifications:**
+ Equivalent education and experience - High School Diploma and 1 years' relevant work experience in clinical research.
+ At least 1 year experience working in a clinical research setting preferred.
+ Working knowledge of clinical trials.
+ Working knowledge of the principles of Good Clinical Practices (GCP).
+ In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
+ Skill in carrying out required clinical procedures.
+ Working knowledge of medical terminology.
+ Ability to pay close attention to detail.
+ Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
+ Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
_Please note, this position is not eligible for sponsorship._
#LI-CES and #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
View Now
8
Clinical Research Site Director
95630 Lake Forest, California
objectivehealth
Posted today
Job Viewed
Job Description
Clinical Research Site DirectorOur clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Site Director. The ideal candidate will possess certification such as RNB, LPN, phlebotomy, or similar, prior clinical research experience, and have a strong desire to work directly with patients. Who We AreObjectiveHealth is a clinical research company that uses proprietary technology to:Increase patient access to research trials within our communities,Provide physicians with enhanced care options for current patients, andDeliver superior clinical research enrollment metrics to Pharma sponsors.All with the goal of Improving Patient Outcomes at the point of care.We want you to join us in doing just that.Who You AreA lover of patient interaction and skilled at providing patient careA team player with a bias for action and an attitude that takes personal responsibilityA proven leader among your peers and teamsSkilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherenceAn expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and othersA strong advocate for Company values, mission, and initiativesNot easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studiesEnergized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology, and/or OncologyWhat Success Looks Like for This RoleTaking ownership of assigned studies and patientsCommunicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correctionShowing up on time, every timeEnsuring strict compliance to the laws, regulations, and requirements of all applicable governing bodiesLearning and using the technologies we provide to enhance your day-to-day activitiesEmbodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and DedicationWhat We OfferCompetitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short- and Long-Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits.RequirementsThis job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant.Compensation for this position is determined based on a combination of factors, including geographic location, relevant experience, and qualifications. Salary Description $82,500 - $107,250
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