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Temporary Clinical Trials Test Subject Jobs (NOW HIRING)

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

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 ...

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 ...

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 ...

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 ...

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

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Temporary Clinical Trials Test Subject information

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$54

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

As of Jul 30, 2026, the average hourly pay for temporary 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 Temporary Clinical Trials Test Subject vs Clinical Research Coordinator?

AspectTemporary Clinical Trials Test SubjectClinical Research Coordinator
CredentialsNo formal certifications typically required; must meet trial-specific criteriaUsually requires a bachelor's degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentParticipates in clinical trials, often in medical facilities or research centersWorks in research sites, hospitals, or clinics managing trial operations
Employer & IndustryPharmaceutical companies, research organizations, hospitalsResearch institutions, hospitals, pharmaceutical companies
Search & Comparison IntentUnderstanding trial participation rolesManaging and coordinating clinical trials

The main difference is that Temporary Clinical Trials Test Subjects participate in trials without requiring extensive certifications, focusing on trial participation. Clinical Research Coordinators, however, manage and oversee the trial process, often needing relevant certifications and experience. Both roles are essential in clinical research but serve different functions within the industry.

More about Temporary Clinical Trials Test Subject jobs
What cities are hiring for Temporary Clinical Trials Test Subject jobs? Cities with the most Temporary 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:
What states have the most Temporary Clinical Trials Test Subject jobs? States with the most job openings for Temporary Clinical Trials Test Subject jobs include:
Infographic showing various Temporary Clinical Trials Test Subject job openings in the United States as of July 2026, with employment types broken down into 84% Full Time, 8% Part Time, and 8% Temporary. Highlights an 100% In-person job distribution, with an average salary of $112,695 per year, or $54.2 per hour.

Subject Mater Expert, Clinical Trials

HCTHealthcare

San Jose, CA

Full-time

Posted 20 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.