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Full Time Clinical Trials Test Subject Jobs (NOW HIRING)

THE ROLE We are seeking a full-time, fully benefited Vitalief employee to serve as a Clinical ... Serve as a subject matter expert for Medicare coverage rules, assisting study teams in identifying ...

... Regular, Full Time Schedule (Monday-Friday, 37.5 Hours per week) Responsibilities : Under the ... The department manager manages staff including clinical trials coordinators, data specialists ...

... Regular, Full Time Schedule (Monday-Friday, 37.5 Hours per week) Responsibilities : Under the ... The department manager manages staff including clinical trials coordinators, data specialists ...

... Regular, Full Time Schedule (Monday-Friday, 37.5 Hours per week) Responsibilities : Under the ... The department manager manages staff including clinical trials coordinators, data specialists ...

Clinical Trials Manager

Raleigh, NC ยท On-site

$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 ...

Clinical Trials Manager

Santa Monica, CA ยท On-site

$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 ...

Clinical Trials Manager

Foster City, CA ยท On-site

$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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Full Time Clinical Trials Test Subject information

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$54

$89

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

As of Aug 8, 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.

More about Full Time Clinical Trials Test Subject jobs
What cities are hiring for Full Time Clinical Trials Test Subject jobs? Cities with the most Full Time 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 Full Time Clinical Trials Test Subject jobs? States with the most job openings for Full Time Clinical Trials Test Subject jobs include:
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 55% Full Time, 27% Part Time, 1% Temporary, and 17% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $112,695 per year, or $54.2 per hour.

CLINICAL RESEARCH COORDINATOR

Clinical Trials Investment Group

Miami, FL โ€ข On-site

$40K - $55K/yr

Full-time

Re-posted 9 days ago


Job description

Clinical Research Site seeking full time clinical research coordinator with experience. Must be Bilingual.

Responsibilities:

  • Must be able to manage an coordinate accordingly
  • Must provide clinical research support to investigators to prepare for and execute assigned research studies including, reviewing protocols, case report forms, study specific documents and electronic data capture systems use to record research data
  • Recruit and screen subjects for clinical trials and maintain all logs
  • Orient research subjects to the study
  • Design and maintain source documentation based on protocol requirements
  • Schedule and Execute study visits and perform all study procedures
  • Collect, Record and maintain research subject study data according to protocol and SOPS
  • Handle lab testing and analysis including preparation of specimen collection tubes and lab logistic
  • Monitor subject safety and report adverse reaction to appropriate medical personnel
  • Trouble shoot study related question and concerns and resolve all queries in a timely manner
  • Attend all IM, SIV and other training session required by the sponsor

Requirements:

  • Must be Bilingual ( English/Spanish)
  • 2+ years of Experience
  • Strong computer skills and knowledgable with medical terminology
  • Knowledge of Office 365
  • Excellent organization skills
  • Excellent written and oral communication skills
  • Excellent Time management
  • ICH and GCP certified

Company Description

WE ARE A GROWING COMPANY WITH VARIOUS DOCTORS SERVING AS PI IN DIFFERENT AREAS OF PRACTICE. WE SPECIALIZE IN CLINICAL TRIALS WE DO NOT OFFER REGULAR MEDICAL SERVICES.