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Overnight Clinical Trials Test Subject Jobs (NOW HIRING)

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Clinical Data Manager 3

San Antonio, TX · 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 ...

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Overnight Clinical Trials Test Subject information

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$22K

$125.3K

$206K

How much do overnight clinical trials test subject jobs pay per year?

As of Sep 6, 2026, the average yearly pay for overnight clinical trials test subject in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What is the difference between Overnight Clinical Trials Test Subject vs Clinical Research Coordinator?

AspectOvernight Clinical Trials Test SubjectClinical Research Coordinator
CredentialsTypically no formal healthcare credentials requiredRequires relevant degrees or certifications in clinical research or healthcare
Work EnvironmentParticipates in clinical trial facilities, often overnight shiftsWorks in research sites, managing study operations during regular hours
Job RoleProvides data by participating in trials, following protocolsCoordinates study activities, manages patient recruitment and data collection

Overnight Clinical Trials Test Subjects focus on participating in trials without requiring healthcare credentials, often during overnight shifts. Clinical Research Coordinators manage study logistics and patient interactions during regular hours. Both roles are essential in clinical research but differ significantly in responsibilities and qualifications.

What cities are hiring for Overnight Clinical Trials Test Subject jobs?

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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 Overnight Clinical Trials Test Subject jobs?

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Overnight Clinical Trials Test Subject jobs near you

Subject Mater Expert, Clinical Trials

HCTHealthcare

San Jose, CA • On-site

Full-time

Re-posted 28 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.