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Full Time Clinical Trials Test Subject Jobs (NOW HIRING)

City of Hope

Clinical Trials Data Coord

Duarte, CA · On-site

This full-time remote position entails ensuring data integrity for various research studies ... Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.

University of Rochester

$64K - $96K/yr

Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400119 Surgery-Cancer Control ... The Clinical Trials Project Manager II for NCORP is responsible for leading the planning ...

Natera

Senior Manager, Clinical Trials

$141K - $176K/yr

This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to support the development, validation, and commercialization non-invasive molecular diagnostic tests.

University of Rochester

$70K - $105K/yr

Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400981 Neuro-Ctr Health & Tech ... Directs and coordinates all aspects of clinical research trials and acts as a liaison to study ...

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How much do full time clinical trials test subject jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for full time clinical trials test subject in the United States is $54.18, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $81.49 per hour, depending on experience, location, and employer.

What is the difference between Full Time Clinical Trials Test Subject vs Part Time Clinical Trials Test Subject?

AspectFull Time Clinical Trials Test SubjectPart Time Clinical Trials Test Subject
Work HoursTypically 40+ hours per weekFewer hours, often flexible or part-time
CredentialsMay require basic health screening, no advanced certificationsSame as full-time, with less commitment
Work EnvironmentResearch facilities, clinics, hospitalsSame as full-time, but with less time commitment
Employer & Industry UsagePharmaceutical companies, research organizationsSame as full-time, often for supplementary income

Full Time Clinical Trials Test Subjects work extensively in research settings, often dedicating full workweeks, while Part Time Clinical Trials Test Subjects participate on a flexible, reduced schedule. Both roles require similar credentials and work environments, but differ mainly in hours and commitment level.

How to become a full time clinical trials test subject?

To become a full-time clinical trials test subject, individuals typically need to meet specific health and demographic criteria, pass medical screenings, and provide informed consent. Participants often sign up through research institutions or clinical trial companies and may need to complete training or assessments related to the study requirements.
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Full Time Clinical Trials Test Subject jobs near you
Infographic showing various Full Time Clinical Trials Test Subject job openings in the United States as of August 2026, with employment types broken down into 58% Full Time, 26% Part Time, 1% Temporary, and 15% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $112,695 per year, or $54.2 per hour.

Clinical Trials Data Coord

City of Hope

Duarte, CA • On-site

Full-time

This job post has expired 2 days ago. Applications are no longer accepted.

City Of Hope rating

8.4

Company rating: 8.4 out of 10

Based on 91 frontline employees who took The Breakroom Quiz

24th of 898 rated healthcare providers

Job description

 
Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. 
This full-time remote position entails ensuring data integrity for various research studies.  Responsibilities include data abstraction, CRF completion, query resolution, sponsor monitor visit coordination, and maintaining audit-ready data.  You will also oversee electronic research records and patient information in the CTMS, contributing to cutting-edge clinical research.
As a successful candidate, you will: 
  • Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations.
  • Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information.
  • Take responsibility for communicating any protocol deviations or issues related to study execution, ensuring transparency and problem resolution.
  • Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements.
  • Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work.
 
Qualifications - External
 
Qualifications - External
 
Qualifications - External
 
Qualifications - External
 
Qualifications - External

Your qualifications should include: 

  • Bachelor's Degree, relevant experience may substitute for degree.
  • At least two years of experience related to the conduct of oncology clinical trials.
  • Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer.

To learn more about our Comprehensive Benefits, please CLICK HERE.

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About City of Hope

Sourced by ZipRecruiter

City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases. Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hopes translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope, a subsidiary launched in 2019 serves employers and their health care partners by providing access to City of Hopes specialized cancer expertise. City of Hope is ranked among the nations Best Hospitals in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.

Industry

Hospitals

Company size

1,001 - 5,000 Employees

Headquarters location

Duarte, CA, US

Year founded

1913

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