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Clinical Trials Test Subject Jobs (NOW HIRING)

Access Community Clinical Trials

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Clinical Research Coordinator II or III

Abilene, TX · On-site

$50K - $64K/yr

Ability to independently manage assigned clinical trials * Knowledge of GCP, FDA regulations, and human subject protections * Experience with EDC, CTMS, eSource, and electronic research systems

Adecco

Clinical Trials Manager- Remote

Chapel Hill, NC · Remote

$62 - $64.73/hr

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of ... An employer who violates this law shall be subject to criminal penalties and civil liability.

Access Community Clinical Trials

Be Seen First

Clinical Research Coordinator II or III

Abilene, TX · On-site

$50K - $64K/yr

Ability to independently manage assigned clinical trials * Knowledge of GCP, FDA regulations, and human subject protections * Experience with EDC, CTMS, eSource, and electronic research systems

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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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Clinical Trials Test Subject jobs near you
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.

Clinical Research Coordinator II or III

Access Community Clinical Trials

Abilene, TX • On-site

$50K - $64K/yr

Full-time

Medical, Dental, Vision, Life, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Access Community Clinical Trials (ACCT) is seeking an experienced Clinical Research Coordinator II or III to join our growing research team in Abilene, Texas. Level will be determined based on experience and demonstrated competencies.

The ideal candidate can independently manage clinical trials while maintaining a strong focus on participant safety, quality data, regulatory compliance, and enrollment performance.

Key Responsibilities

  • Independently coordinate clinical trials from start-up through closeout
  • Conduct protocol-required study visits and maintain accurate source documentation
  • Recruit, screen, enroll, and retain study participants
  • Conduct and document informed consent discussions
  • Perform vital signs, EKGs, venipuncture, and laboratory specimen processing/shipping
  • Enter study data into EDC systems and resolve queries within required timelines
  • Identify, document, and report AEs/SAEs appropriately
  • Maintain investigational product accountability and temperature monitoring
  • Coordinate monitoring visits and sponsor/CRO communications
  • Maintain study records in an audit-ready state
  • Ensure compliance with protocols, FDA regulations, ICH-GCP, sponsor requirements, and ACCT SOPs

Qualifications

CRC II

  • Minimum 2 years of clinical research coordination experience
  • Ability to independently manage assigned clinical trials
  • Knowledge of GCP, FDA regulations, and human subject protections
  • Experience with EDC, CTMS, eSource, and electronic research systems
  • Strong clinical, organizational, and documentation skills

CRC III

  • Advanced experience independently managing multiple clinical trials
  • Strong recruitment and enrollment experience
  • Experience mentoring or training research staff
  • Experience with sponsor monitoring visits, audits, feasibility assessments, and site qualification activities
  • Strong leadership, problem-solving, and study management skills

CCRC, CCRP, or equivalent certification is preferred but not required.

Competitive salary and benefits provided

About ACCT

Access Community Clinical Trials partners with physicians and healthcare organizations to bring clinical research opportunities into local communities.

Our priorities are simple: Participant Safety. Quality Data. Ethical Research Practices.

If you are an experienced CRC looking for an opportunity to take ownership of your studies and grow with an expanding clinical research organization, we encourage you to apply.

Company Description

At Access Community Clinical Trials (ACCT), you'll be part of a team dedicated to bringing innovative clinical research opportunities directly to local communities. We believe patients should have access to cutting-edge treatments close to home, and our team plays a vital role in making that possible. ACCT offers a collaborative, mission-driven environment where employees are valued, supported, and empowered to grow professionally. Our team members have the opportunity to make a meaningful impact on medical advancement while building strong relationships with investigators, sponsors, and participants. If you are seeking a rewarding career where your work improves lives, supports scientific innovation, and contributes to the future of healthcare, ACCT is the place for you.