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Clinical Trials Test Subject Jobs (NOW HIRING)

asrcfh

Clinical Data Manager 2

Reston, VA · On-site

Test new processes and systems for the management of data in clinical trials * Test clinical trial databases and data entry screens assuring compliance with protocol and institutional processes and ...

asrcfh

Clinical Data Manager 2

Reston, VA · On-site

Test new processes and systems for the management of data in clinical trials * Test clinical trial databases and data entry screens assuring compliance with protocol and institutional processes and ...

Vitalief

Clinical Trials Coverage Analyst

Chicago, IL · Remote

$70K - $85K/yr

Serve as a subject matter expert for Medicare coverage rules, assisting study teams in identifying ... Test (TST) for Mycobacterium Tuberculosis. #LI-DNP Powered by JazzHR rDpvGBgzgt

Kite Pharma

Clinical Trials Manager

Santa Monica, CA

$146K - $189K/yr

As a Clinical Trials Manager at Gilead/Kite, you will be responsible for: * Coordinating and ... Eligible employees may participate in benefit plans, subject to the terms and conditions of the ...

Kite Pharma

Clinical Trials Manager

Raleigh, NC

$146K - $189K/yr

As a Clinical Trials Manager at Gilead/Kite, you will be responsible for: * Coordinating and ... Eligible employees may participate in benefit plans, subject to the terms and conditions of the ...

Exelixis

Clinical Trials Manager (Oncology)

Alameda, CA · On-site

The Clinical Trials Manager (CTM), Clinical Operations, coordinates the activities associated with ... and subject instructions • May participate in strategic governance discussions as required (e.g ...

Kite Pharma

Clinical Trials Manager

Foster City, CA

$146K - $189K/yr

As a Clinical Trials Manager at Gilead/Kite, you will be responsible for: * Coordinating and ... Eligible employees may participate in benefit plans, subject to the terms and conditions of the ...

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Clinical Trials Test Subject information

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

As of Jul 19, 2026, the average hourly pay for clinical trials test subject in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is a Clinical Trials Test Subject job?

A Clinical Trials Test Subject participates in medical research studies to help test the safety and effectiveness of new treatments, medications, or medical devices. Subjects may undergo various tests, treatments, or monitoring under the supervision of healthcare professionals. Participation is voluntary, and subjects are informed of potential risks and benefits before enrolling. Compensation, requirements, and study duration vary depending on the trial.

How to recruit subjects for clinical trials?

Recruiting subjects for clinical trials involves identifying eligible participants through outreach methods such as advertisements, healthcare provider referrals, and community engagement. Ensuring proper screening, informed consent, and adherence to ethical guidelines are essential steps in the recruitment process for clinical trial staff or coordinators.

What jobs are there in clinical trials?

Jobs in clinical trials include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications.

How much money do test subjects make?

Clinical trials test subjects typically earn between $50 and $3,000 per study, depending on the trial's length, complexity, and risk level. Compensation can vary based on factors such as health requirements, the type of medication or procedure involved, and the time commitment required for participation.

What are the key skills and qualifications needed to thrive in the Clinical Trials Test Subject position, and why are they important?

To thrive as a Clinical Trials Test Subject, you need to meet specific health and demographic criteria, have reliable transportation, and be willing to follow detailed study protocols. Familiarity with basic health assessments and the ability to use electronic diaries or monitoring devices are sometimes required. Dependability, attention to detail, and clear communication with research staff are valuable soft skills in this role. These qualities ensure the accuracy of trial data, participant safety, and smooth execution of clinical research studies.

What should I expect during a typical day as a Clinical Trials Test Subject?

As a Clinical Trials Test Subject, your day may involve undergoing scheduled medical tests, taking investigational medication or using new devices, and closely following instructions provided by research staff. You might spend time at a research facility for monitoring or complete tasks at home such as logging symptoms or side effects in an electronic diary. Interactions with clinical coordinators and regular health check-ins are common, ensuring your safety and accurate data collection. The environment is typically supportive, structured, and geared toward maintaining participant comfort and well-being throughout the study.

More about Clinical Trials Test Subject jobs
What cities are hiring for Clinical Trials Test Subject jobs? Cities with the most Clinical Trials Test Subject job openings:
What are the most commonly searched types of Clinical Trials Test Subject jobs? The most popular types of Clinical Trials Test Subject jobs are:
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Clinical Trials Test Subject jobs near you
Infographic showing various Clinical Trials Test Subject job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Subject Mater Expert, Clinical Trials

HCTHealthcare

San Jose, CA

Full-time

Posted 9 days ago

Job description

HCT is seeking an interim Clinical Trials Subject Matter Expert for a 240+ bed hospital in California.

The responsibilities include:

  • With direction from the PI, this position coordinates research activities. This position is also responsible for protecting the health, safety, and welfare of research participants.
  • Must be proficient in electronic health systems and databases used in research environment, or willingness to learn and demonstrate proficiency within six months of hire.

Requirements:

  • Education: Minimum of a diploma from an accredited nursing school required. High School Diploma or General Education Development (GED) required.
  • Experience: Minimum two (2) years of clinical nursing experience in a hospital, clinic or similar health care setting within the last three (3) years required (Bachelor's degree may be substituted for one (1) year work experience).
  • License: Registered Nurse License (California). Basic Life Support
  • EMR: Epic

Expenses are covered while on assignment including housing, airfare, and rental car.

Earn $2,000 for every candidate or position placement from your referral that HCT successfully places! Submit Referral Here

Keywords: Subject Matter Expert (SME), Clinical Trial Subject Matter Expert, Clinical Research Consultant, Clinical Research Manager, Clinical Trial Manager (CTM), Senior Clinical Trial Manager, Clinical Operations Manager, Director of Clinical Operations, Associate Director of Clinical Operations, Clinical Program Manager, Clinical Project Manager, Clinical Development Manager, Clinical Research Scientist, Clinical Scientist, Medical Affairs Manager, Research Nurse, Clinical Research Coordinator (CRC), Clinical Research Associate (CRA), Principal CRA, Clinical Trial Lead, Clinical Trials, Clinical Research, Clinical Operations, Phase I, Phase II, Phase III, Phase IV, Investigator-Initiated Trials (IIT), Multicenter Studies, Global Clinical Trials, Site Management, Trial Startup, Study Start-Up, Patient Recruitment, Site Activation, Clinical Monitoring.