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Clinical Trials Jobs (NOW HIRING)

This role is responsible for overseeing the operational execution of clinical trials, ensuring compliance with regulatory requirements, optimizing research processes, and supporting cross-functional ...

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Wahl. The relevant individual will also work on diagnostic imaging trials led by Dr. Wahl, working with the Center for Clinical Imaging Research. The position is directly responsible for the ...

Summary With oversight from the responsible Clinical Trials Office Manager, and in collaboration with the faculty and investigators, the Clinical Trials (CTO) Supervisor provides basic day-to-day ...

Summary With oversight from the responsible Clinical Trials Office Manager, and in collaboration with the faculty and investigators, the Clinical Trials (CTO) Supervisor provides basic day-to-day ...

Clinical Trials Manager

$133K - $172K/yr

May serve as a resource for others within the company for clinical trials management expertise. * Under general supervision, is able to examine functional issues from an organizational perspective.

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Clinical Trials information

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$28

$62

$96

How much do clinical trials jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for clinical trials 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 are the key skills and qualifications needed to thrive in the Clinical Trials position, and why are they important?

To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.

How to get into clinical trial work?

To work in clinical trials, individuals typically need a background in healthcare, life sciences, or related fields, along with relevant certifications such as Good Clinical Practice (GCP). Entry-level roles often require strong organizational skills, attention to detail, and familiarity with regulatory requirements; some positions may also require a bachelor's degree or higher. Gaining experience through internships or training programs can improve job prospects in this field.

How much money can I make doing clinical trials?

Clinical trial participants can earn anywhere from $50 to several thousand dollars depending on the study's duration, complexity, and requirements. Compensation varies based on factors such as the type of trial, location, and whether medical procedures or tests are involved. Participants often receive payment after completing the study or specific milestones within it.

Which clinical trials pay the most?

Clinical trials involving high-risk or complex treatments, such as oncology or rare disease studies, often offer higher compensation to participants and staff. Additionally, roles like clinical research coordinators or principal investigators in well-funded trials tend to earn more due to their responsibilities and expertise. Compensation varies based on trial phase, location, and the level of experience required.

What are some common career paths or advancement opportunities for professionals working in Clinical Trials?

Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.

Are clinical trial jobs in high demand?

Clinical trial jobs are in high demand due to the ongoing need for new medical treatments and the growth of the healthcare industry. Positions such as clinical research coordinators and data managers are often sought after, especially for those with relevant certifications and experience in regulatory compliance and data management tools.

What is a Clinical Trials job?

A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

What cities are hiring for Clinical Trials jobs? Cities with the most Clinical Trials job openings:
What are the most commonly searched types of Clinical Trials jobs? The most popular types of Clinical Trials jobs are:
What states have the most Clinical Trials jobs? States with the most job openings for Clinical Trials jobs include:
Infographic showing various Clinical Trials job openings in the United States as of June 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.
Clinical Trials System Administrator

Clinical Trials System Administrator

Westchester Medical Center

Valhalla, NY โ€ข On-site

Full-time

Posted 17 days ago


Job description

Responsible for the application support and maintenance activities of the clinical research applications utilized at CRHI and across the Network. ย  This individual assists with training staff in the use of these systems and coordinates reporting needs. ย 

Responsibilities:ย 

  • Perform in depth analysis of research operation workflows and data collection methods.
  • Create workflow diagrams and step-by-step process documentation.
  • Identify opportunities for process optimization and implement solutions.
  • Participate in the integration efforts between the Network Clinical Trials Management System and other clinical operating systems (i.e. EPIC).ย 
  • Consult and collaborate with the clinical research management teams to review reporting needs.ย 
  • Prepare reports and dashboards; run ad hoc queries.
  • Assist in testing and system validation.

Qualifications/Requirements:

Experience: ย 

  • Five years of experience in systems analysis and application program development.
  • Proficient in Microsoft Excel.
  • Knowledge of Microsoft Visio preferred.
  • Knowledge of Tableau preferred.
  • Knowledge of OnCore/Clinical Trials Management Systems preferred.
  • Knowledge of EPIC preferred.

Education: ย 

Bachelorโ€™s Degree or equivalent combination of education, training and/or experience that demonstrates the ability to perform the duties of the position

Licenses / Certifications: ย 

Other:ย