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Clinical Research Project Coordinator Jobs in Riverside, CA

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Clinical Research Project Coordinator information

See Riverside, CA salary details

$23.5K

$66.1K

$97K

How much do clinical research project coordinator jobs pay per year?

As of Aug 31, 2026, the average yearly pay for clinical research project coordinator in Riverside, CA is $66,107.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,800.00 and $74,100.00 per year, depending on experience, location, and employer.

What does a clinical research project coordinator do?

A Clinical Research Project Coordinator manages and oversees the daily operations of clinical research studies. Their responsibilities include coordinating study activities, ensuring compliance with regulatory requirements, maintaining accurate documentation, scheduling participant visits, and communicating with research teams and sponsors. They play a crucial role in ensuring that research projects run smoothly, on time, and within budget while upholding ethical standards.

What are the key skills and qualifications needed to thrive as a clinical research project coordinator?

To thrive as a Clinical Research Project Coordinator, you need a solid understanding of clinical research methodologies, project management, and regulatory compliance, typically supported by a bachelor’s degree in a health or science field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like CCRC or CCRP are commonly required. Exceptional organizational skills, attention to detail, and strong interpersonal communication help manage timelines, collaborate with stakeholders, and ensure protocol adherence. These competencies are crucial for maintaining study integrity, meeting regulatory standards, and ensuring successful project delivery in complex research environments.

What are some common challenges faced by clinical research project coordinators, and how can they be managed effectively?

Clinical Research Project Coordinators often encounter challenges such as balancing multiple studies simultaneously, ensuring regulatory compliance, and maintaining clear communication among diverse stakeholders. Effective time management, attention to detail, and the ability to adapt to changing protocols are essential in this role. Building strong relationships with research staff, principal investigators, and sponsors can help streamline processes and resolve issues quickly. Staying organized and proactively addressing potential obstacles can significantly contribute to the success of clinical research projects.

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

AspectClinical Research Project CoordinatorClinical Research Associate
CredentialsBachelor's degree in life sciences or related field; certifications like CCRP are a plusTypically requires similar degrees; certifications like CRA or CCRP are common
Work EnvironmentManages study logistics, coordinates with teams, and oversees daily activities at research sitesMonitors clinical trials, ensures compliance, and conducts site visits
Employer & Industry UsageUsed by hospitals, research institutions, and pharmaceutical companies for study coordinationPrimarily employed by CROs, pharmaceutical companies, and biotech firms for trial monitoring

While both roles support clinical research, the Clinical Research Project Coordinator focuses on managing study operations and logistics, whereas the Clinical Research Associate primarily monitors trial compliance and site performance. Both roles require similar educational backgrounds and certifications, but their daily responsibilities and work environments differ.

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

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

What are popular job titles related to Clinical Research Project Coordinator jobs in Riverside, CA?

For Clinical Research Project Coordinator jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Clinical Research Project Coordinator jobs in Riverside, CA look for?

The top searched job categories for Clinical Research Project Coordinator jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Clinical Research Project Coordinator jobs?

Cities near Riverside, CA with the most Clinical Research Project Coordinator job openings:

Clinical Research Project Coordinator jobs near you
Infographic showing various Clinical Research Project Coordinator job openings in Riverside, CA as of June 2026, with employment types broken down into 3% As Needed, 48% Full Time, 33% Part Time, 1% Temporary, and 15% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $66,107 per year, or $31.8 per hour.

Clinical Project Coordinator

Motion Recruitment Partners, LLC

Irvine, CA • On-site

Other

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago

Job description

Clinical Project Coordinator
Kelly Science and Clinical FSP is currently seeking a Clinical Project Coordinator for a remote opportunity supporting our Medical Device client. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you will be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You will also be eligible for paid time off, including holiday, vacation, and sick/personal time.
Summary:
This individual will provide support to the clinical study staff
Perform a variety of clinical research operations duties of a routine and technical nature in support of clinical trials. This includes tracking study documents and management of the Trial Master File (v-TMF).
Supports project managers within the assigned clinical studies.
Key Job Activities:
  • Accountable for tracking essential documents and ensuring completeness of the v-TMF.
  • Assist study staff and Administrative Clinical Study Administrators (aCSA) to quickly resolve issues relating to the v-TMF. Identifies problems and assists in implementing corrective and preventive actions.
  • Manages and supports ongoing use of the Clinical Trial Management System (CTMS) and tracking study milestones and activities.
  • Provide safety documentation to other functional groups in support of safety committee meetings as requested.
  • As directed, provides support to the project teams which may include tracking study data, following-up with clinical sites on essential documents; assist in drafting and distributing study mailings, including study newsletters; assist in drafting of agenda/meeting minutes and scheduling of meetings; assist in providing internal communication of important clinical data and events.
  • Assist with tracking site payments.
  • Performs data entry in systems
  • Run reports including training matrix reports, metrics for management reviews.
  • Support management of IRB/IEC renewal compliance.
  • Coordinate process for the review of study data, such as MRIs, by third-party vendors.
  • Assist in ordering, shipping, tracking of, study supplies including, but not limited to, investigational devices and site binders.
  • Maintain master device accountability log as requested.
  • Assist with scheduling and organizing investigators and expert panel meetings.
  • Assist with file reviews and Audit preparation.
  • Responsible for ensuring appropriate level of communication with managers, project leaders, and team members.
  • Work with management group to help achieve department goals.
  • Participate in process improvement activities within the department, including process improvement activities related to the v-TMF/CTMS.
  • May be involved in other tasks to support the Scientific Affairs Clinical department and Operating Company as needed.

Education:
Minimum of a Bachelor's Degree is required.
Experience
Previous clinical research experience preferred
Requires previous administrative support experience or equivalent for at least 1 year.
Clinical/medical background preferred
Knowledge
Requires experience and knowledge working with computer systems (Microsoft office - Excel, Word and Power Point). Demonstrated competencies in the following areas are required:
Tracking
Written and verbal communications
Attention to details
Organizational skills

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