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Clinical Research Project Assistant Jobs (NOW HIRING)

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How much do clinical research project assistant jobs pay per hour?

As of Jul 8, 2026, the average hourly pay for clinical research project assistant in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What do clinical research assistants do?

Clinical research assistants support the conduct of clinical trials by preparing study materials, recruiting and screening participants, collecting and managing data, and ensuring compliance with protocols and regulations. They often work under the supervision of investigators and may use electronic data capture tools or databases as part of their responsibilities.

What is the difference between Clinical Research Project Assistant vs Clinical Research Coordinator?

AspectClinical Research Project AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCR are common
Work EnvironmentSupports research teams in clinical settings, hospitals, or research institutionsManages daily clinical trial activities, interacts directly with patients and investigators
Employer & Industry UsageUsed by research institutions, hospitals, pharmaceutical companiesCommonly employed in clinical trial sites, hospitals, and research organizations

The Clinical Research Project Assistant primarily supports research activities and data management, while the Clinical Research Coordinator oversees trial operations and patient interactions. Both roles require similar educational backgrounds and certifications, but their responsibilities differ in scope and daily tasks.

How much money do clinical research assistants make?

Clinical research assistants typically earn a median annual salary of around $45,000 to $55,000, depending on experience, location, and the complexity of the research environment. Entry-level positions may start lower, while those with specialized skills or certifications can earn higher wages.

What does a research project assistant do?

A research project assistant supports the planning, coordination, and execution of clinical research studies. They handle tasks such as data collection, maintaining study documentation, scheduling participant visits, and ensuring compliance with protocols and regulations. Strong organizational skills and familiarity with research tools like electronic data capture systems are often required.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, such as a background in healthcare or life sciences, and often involves monitoring clinical trials. Entry-level roles in clinical research may include Clinical Trial Assistant or Research Coordinator, with CRAs generally needing several years of related experience or specialized training. Certifications like SOCRA or ACRP can also be beneficial for advancing to CRA roles.
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What cities are hiring for Clinical Research Project Assistant jobs? Cities with the most Clinical Research Project Assistant job openings:
What are the most commonly searched types of Clinical Research Project jobs? The most popular types of Clinical Research Project jobs are:
What states have the most Clinical Research Project Assistant jobs? States with the most job openings for Clinical Research Project Assistant jobs include:

Research Project Assistant

UPMC Senior Communities

Pittsburgh, PA โ€ข On-site

$20.20 - $32.01/hr

Full-time

Posted 13 days ago


Job description

The Center for Women's Biobehavioral Health Research (PI: Rebecca Thurston) is devoted to understanding and enhancing women's health at midlife and beyond. The Center, located in Sterling Plaza, is within the Department of Psychiatry at the University of Pittsburgh. The Research Project Assistant plays a key role in the execution and coordination of studies at the Center including the Study of Women Across the Nation and an industry sponsored menopause study. The trial examines the effects of a prescription treatment for menopausal hot flashes on brain, cognitive, and vascular function in midlife women.
This position requires prior experience supporting clinical trials or clinical research studies, and demonstrated proficiency in protocol-driven study operations, participant safety procedures, and regulatory documentation. The Research Project Assistant will work closely with the Study Coordinator, and investigative team to ensure accurate and compliant study conduct. Experience with regulatory documentation, phlebotomy, cognitive testing, wearable devices, and/or clinical research involving women's health and/or menopause is highly preferred.
This position is grant funded.
Responsibilities:
  • Recruit, screen, and enroll study participants, including explaining the research protocol and obtaining informed consent for study screening activities in accordance with IRB-approved procedures.
  • Assist with all aspects of the FAVES-B study protocol, serving as a point of contact for study participants.
  • Administer structured interviews and cognitive assessment batteries, obtain physical measures, train participants on wearable devices, and escort participants to assessments conducted at other laboratories on campus.
  • Process blood and related biological samples, including Venipuncture and blood collection from participants, preparation of study equipment and phlebotomy tubes, sample labeling, handling, storage, and transport to designated laboratories in compliance with protocol and safety requirements.
  • Enter data in study databases.
  • Perform other duties as assigned in support of the research program and study objectives.

Qualifications:
  • Bachelor's degree required, preferably in Psychology, Neuroscience, Sociology or related research field.
  • Minimum of 2 years of work experience in a research project and/or related clinical setting is required.
  • Familiarity with computers and common software packages required.
  • Working knowledge of research methodology strongly preferred.
  • Prior supervisory and/or project management experience preferred.

Licensure, Certifications, and Clearances:
  • Act 34

UPMC is an Equal Opportunity Employer/Disability/Veteran