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Clinical Trials Part Time Jobs in Riverside, CA (NOW HIRING)

City of Hope

Security Officer, Part time OC

Irvine, CA

$17.25 - $20.50/hr

... clinical trials, and holistic services such as rehabilitative therapy and spiritual care. This isn ... This is a part time position working Sundays and Mondays 6:00 a.m. to 2:30 p.m. The Security ...

City of Hope

Security Officer, Part time OC

Irvine, CA

$17 - $20.25/hr

... clinical trials, and holistic services such as rehabilitative therapy and spiritual care. This isn ... This is a part time position working Sundays and Mondays 6:00 a.m. to 2:30 p.m. The Security ...

City of Hope

Social Worker III

Irvine, CA

Clinical Social Worker III - Orange County Part time weekends/Saturday About City of Hope Orange ... trials, and holistic services such as rehabilitative therapy and spiritual care. This isn't ...

City of Hope

Social Worker III

Irvine, CA

Clinical Social Worker III - Orange County Part time weekends/Saturday About City of Hope Orange ... trials, and holistic services such as rehabilitative therapy and spiritual care. This isn't ...

All JobsClinical Trials JobsClinical Trials Part Time JobsClinical Trials Part Time Jobs in Riverside, CA

Clinical Trials Part Time information

See Riverside, CA salary details

$30

$65

$100

How much do clinical trials part time jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for clinical trials part time in Riverside, CA is $65.22, according to ZipRecruiter salary data. Most workers in this role earn between $52.93 and $73.46 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in a part-time clinical trials role, and why are they important?

To thrive in a part-time clinical trials role, you typically need a background in life sciences or healthcare, attention to detail, and familiarity with clinical research protocols. Experience with electronic data capture (EDC) systems, knowledge of Good Clinical Practice (GCP), and sometimes certification such as SOCRA or ACRP are commonly required. Strong organizational skills, clear communication, and adaptability help you excel in coordinating studies and working with diverse teams. These skills ensure accurate data collection, regulatory compliance, and efficient support of clinical research objectives.

What is a clinical trials part time job?

Clinical trials part time jobs are positions in which individuals assist with the planning, execution, or management of clinical research studies on a part-time basis. These roles may include research assistants, coordinators, data managers, or nurses, and offer flexible work hours to accommodate other commitments. Part-time staff are crucial in supporting the collection and management of data, participant recruitment, and ensuring compliance with study protocols. These positions are ideal for students, professionals seeking flexible hours, or those looking to gain experience in clinical research without committing to a full-time schedule.

What are the common responsibilities and challenges of working part-time in clinical trials?

Part-time roles in clinical trials typically involve supporting research coordinators, assisting with data collection and entry, participant recruitment, and ensuring compliance with study protocols. A common challenge can be balancing workload and communication with the team, as studies often require careful coordination and timely updates. Flexibility and strong organizational skills are important, as part-time staff may need to quickly adapt to changing priorities while maintaining high-quality standards. Despite these challenges, part-time positions offer valuable exposure to clinical research processes and can serve as a stepping stone to full-time roles or advanced positions in the field.

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

AspectClinical Trials Part TimeClinical Research Coordinator
CredentialsTypically requires a degree in health sciences or related field; certifications like CCRP are a plusRequires a degree in health sciences or related field; often holds certifications such as CCRP or CCRC
Work EnvironmentPart-time roles in clinics, hospitals, or research facilities; flexible schedulesFull-time or part-time roles in research sites, hospitals, or pharmaceutical companies
Employer & IndustryPharmaceutical companies, CROs, academic institutionsResearch sites, hospitals, pharmaceutical companies

Clinical Trials Part Time roles focus on supporting specific trial activities with flexible hours, while Clinical Research Coordinators oversee entire study processes, often working full-time. Both roles require similar credentials and are integral to clinical research, but differ mainly in scope and schedule.

What are the most commonly searched types of Clinical Trials jobs in Riverside, CA?

The most popular types of Clinical Trials jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Clinical Trials Part Time jobs?

Cities near Riverside, CA with the most Clinical Trials Part Time job openings:

Clinical Trials Part Time jobs near you
Infographic showing various Clinical Trials Part Time job openings in Riverside, CA as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $135,661 per year, or $65.2 per hour.

Part-time Psychiatrist - Clinical Research

Headlands Research

Riverside, CA

Part-time

Re-posted 19 hours ago

Job description

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.

The Role of a Lifetime

Are you ready to make a difference? We're seeking a part-time experienced psychiatrist to help us grow our clinical research site at Artemis Institute for Clinical Research in Riverside, CA. Ideally, this person would work up to any 3 days per week Monday through Thursday, during the hours of 8:00am to 2:00pm. 

Responsibilities:

  • Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:

  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials is a huge plus, but willing to consider those without.
  • Eligible for or active unencumbered license to practice as an MD or DO within the state of California required
  • Must be board-certified or board-eligible.
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.

Apply