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Clinical Research Assistant Part Time Jobs (NOW HIRING)

MPF Federal

Research Assistant - Part Time

Bethesda, MD · On-site +1

$28K - $30K/yr

Perform duties under the direction of the clinical research managers and more experienced staff ... requirements. • Assist in the development of client deliverables according to project ...

University of Utah

Hourly Research Assistants

Campus, IL

$13.82 - $26.94/hr

No Standard Hours per Week 20 Full Time or Part Time? Part Time Shift Day Work Schedule Summary ... Responsibilities Research Assistant, I Administrative tasks in support of the clinical research ...

University of Utah

Hourly Research Assistants

Campus, IL · On-site

$13.82 - $26.94/hr

No Standard Hours per Week 20 Full Time or Part Time? Part Time Shift Day Work Schedule Summary ... Responsibilities Research Assistant, I Administrative tasks in support of the clinical research ...

University of Utah

Hourly Research Assistants

Campus, IL

$13.82 - $26.94/hr

No Standard Hours per Week 20 Full Time or Part Time? Part Time Shift Day Work Schedule Summary ... Responsibilities Research Assistant, I Administrative tasks in support of the clinical research ...

University of Utah

Hourly Research Assistants

Campus, IL · On-site

$10.92 - $25.20/hr

Yes Standard Hours per Week 19 Full Time or Part Time? Part Time Shift Day Work Schedule Summary Is ... Research Assistant, I administrative tasks in support of the clinical research program or ...

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Clinical Research Assistant Part Time information

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How much do clinical research assistant part time jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for clinical research assistant part time in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.

What does a Clinical Research Assistant Part Time do?

A Clinical Research Assistant Part Time supports clinical studies by helping with data collection, patient recruitment, and maintaining study documentation. They work under the supervision of clinical research coordinators or principal investigators, ensuring that research protocols are followed and data is accurately recorded. Their part-time role allows them to contribute to research projects while balancing other commitments, such as school or another job.

What are the key skills and qualifications needed to thrive as a Clinical Research Assistant Part Time, and why are they important?

To thrive as a Clinical Research Assistant Part Time, you need a background in life sciences or health-related fields, attention to detail, and strong organizational abilities. Familiarity with data management systems, regulatory compliance (such as GCP), and basic statistical software is typically required. Excellent communication, teamwork, and problem-solving skills help you coordinate effectively with research teams and study participants. These competencies ensure accurate data collection, regulatory adherence, and smooth operation of clinical trials.

What do we mean by clinical?

In the context of a Clinical Research Assistant role, 'clinical' refers to activities related to patient care, medical testing, and the study of health conditions within healthcare settings. It involves working with clinical trial protocols, collecting data, and ensuring compliance with regulatory standards. Understanding clinical procedures and maintaining accurate documentation are essential skills for this position.

What does it mean for someone to be clinical?

Being clinical typically refers to working in a healthcare or research setting involving patient care, medical assessments, or clinical trials. For a Clinical Research Assistant, it means assisting with the conduct of clinical studies, collecting data, and ensuring compliance with protocols and regulations.

What is the difference between Clinical Research Assistant Part Time vs Clinical Research Coordinator?

AspectClinical Research Assistant Part TimeClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; often holds certifications such as CCRP or CCRP-CR
Work EnvironmentAssists in data collection, patient interactions, and administrative tasks; part-time hoursManages study protocols, patient recruitment, and regulatory compliance; full-time or part-time
Employer & Industry UsageUsed by hospitals, research institutes, and pharmaceutical companies for supporting clinical trialsEmployed in similar settings, often overseeing entire study processes

While both roles support clinical research, the Clinical Research Assistant Part Time typically focuses on data collection and administrative tasks on a part-time basis, whereas the Clinical Research Coordinator manages study operations and patient interactions, often working full-time. The roles share similar credentials and work environments but differ mainly in scope and hours.

What are some common challenges faced by part-time Clinical Research Assistants, and how can they be addressed?

Part-time Clinical Research Assistants often face the challenge of balancing multiple projects and shifting priorities within a limited number of work hours. Communication and organization are key to staying aligned with full-time team members and ensuring that critical research tasks are completed on schedule. Proactively coordinating with the principal investigator and other study staff can help clarify expectations and integrate your contributions effectively. Utilizing project management tools and regularly attending team meetings, even virtually, can also help you stay updated and contribute meaningfully.

What is the movie clinical about?

There is no widely known movie titled 'Clinical.' If referring to a film with a similar name, it typically involves themes related to medical or psychological treatment. For a clinical research assistant, understanding medical or clinical themes can be helpful, but specific movie details are not relevant to the role.

What does very clinical mean?

In the context of a Clinical Research Assistant, 'very clinical' typically refers to work that involves direct interaction with patient data, clinical procedures, or medical environments. It indicates a focus on clinical protocols, patient safety, and adherence to healthcare standards, often requiring knowledge of medical terminology and possibly certifications like Good Clinical Practice (GCP).
More about Clinical Research Assistant Part Time jobs
What cities are hiring for Clinical Research Assistant Part Time jobs? Cities with the most Clinical Research Assistant Part Time job openings:
What states have the most Clinical Research Assistant Part Time jobs? States with the most job openings for Clinical Research Assistant Part Time jobs include:
What job categories do people searching Clinical Research Assistant Part Time jobs look for? The top searched job categories for Clinical Research Assistant Part Time jobs are:
Clinical Research Assistant Part Time jobs near you
Infographic showing various Clinical Research Assistant Part Time job openings in the United States as of June 2026, with employment types broken down into 93% Full Time, and 7% Part Time. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $42,079 per year, or $20.2 per hour.

Clinical Research Assistant (Must live in Los Angeles and Speak Spanish)

Angel City VA

Los Angeles, CA • On-site

Part-time

Posted 29 days ago

Job description

Title: Part time Clinical Research assistant
Job Summary:
The Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Essential Responsibilities and Duties:
• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
• Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
• Assisting Coordinators in assessments, blood pressure, urine collection, draw labs
• Communicating with study participants, caregivers, third party vendors and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
• Office/administrative tasks assigned ie: resupplying exam rooms, ordering office supplies, answering phone calls, etc.
Education/Experience/Skills:
• High school graduate or equivalent. Bac
• Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
• Skilled in organization and record maintenance.
• Strong personal initiative and attention to detail.
• Ability to clearly communicate both orally and verbally.
• Prior experience in healthcare, research, or clinical settings is a plus.
• Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus.

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