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Clinical Trials Test Subject Jobs (NOW HIRING)

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.

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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 Aug 21, 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?

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.

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.

What are the key skills and qualifications needed to thrive as a clinical trials test subject?

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.

How to become a clinical trials test subject?

To become a clinical trials test subject, individuals typically need to meet specific health and demographic criteria outlined in the study's inclusion and exclusion guidelines. Interested participants usually sign up through research institutions or clinical trial registries, and may be required to undergo health screenings and provide informed consent before participation.

How to recruit subjects for clinical trials?

Recruiting subjects for clinical trials involves advertising through clinics, hospitals, and community outreach, as well as using databases of potential participants. Ensuring proper screening and informed consent is essential to select eligible volunteers. Recruitment often requires collaboration with healthcare providers and adherence to ethical guidelines.
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What states have the most Clinical Trials Test Subject jobs?

States with the most job openings for Clinical Trials Test Subject jobs include:

Infographic showing various Clinical Trials Test Subject job openings in the United States as of August 2026, with employment types broken down into 58% Full Time, 25% Part Time, and 17% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% 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

Re-posted 12 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.