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Clinical Research Program Manager Jobs in Riverside, CA

M3USA

Clinical Research Coordinator

Irvine, CA

$30 - $40/hr

With close to 30 owned and managed research sites across the country, M3 Wake Research is one of ... Employee assistance program * Flexible spending account * Health insurance * Life insurance * Paid ...

M3USA

Clinical Research Coordinator

Irvine, CA · On-site

$30 - $40/hr

With close to 30 owned and managed research sites across the country, M3 Wake Research is one of ... Employee assistance program * Flexible spending account * Health insurance * Life insurance * Paid ...

M3USA

Clinical Research Coordinator

Irvine, CA · On-site

$30 - $40/hr

With close to 30 owned and managed research sites across the country, M3 Wake Research is one of ... Employee assistance program * Flexible spending account * Health insurance * Life insurance * Paid ...

Ossur

Clinical Research Scientist

Irvine, CA · On-site

You will manage the planning and execution of clinical studies for products from conception through ... Clinical Research Management: * Design, implementation, and manage internal clinical research ...

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Clinical Research Program Manager information

See Riverside, CA salary details

$46.4K

$96.6K

$156K

How much do clinical research program manager jobs pay per year?

As of May 31, 2026, the average yearly pay for clinical research program manager in Riverside, CA is $96,610.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,600.00 and $109,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Program Manager, and why are they important?

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.

What are some typical challenges faced by Clinical Research Program Managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

What does a Clinical Research Program Manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

What is the difference between Clinical Research Program Manager vs Clinical Research Coordinator?

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What are popular job titles related to Clinical Research Program Manager jobs in Riverside, CA? For Clinical Research Program Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Program Manager jobs in Riverside, CA look for? The top searched job categories for Clinical Research Program Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Clinical Research Program Manager jobs? Cities near Riverside, CA with the most Clinical Research Program Manager job openings:
Clinical Research Program Manager jobs near you

Senior Clinical Research Coordinator

Headlands Research

Riverside, CA

$76K - $90K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 29 days ago

Job description

Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more than 50 years of combined research experience, Artemis specializes in Psychiatry/Neurology, Internal Medicine, and Women's Health studies. With multiple locations serving Southern California, including San Diego and Riverside, each Artemis site is fully equipped to conduct complex clinical research trials. 

Want to be a part of a growing company that's making a difference in our world? Look no further than Artemis Institute for Clinical Research! You'll enjoy a friendly and exciting culture with opportunities for growth and advancement. We offer the following generous benefits to our full-time employees:

  • A range of PPO and HMO medical plans
  • PPO and HMO dental plans
  • Vision coverage, long term disability plan, and life/AD&D coverage
  • 401k plan
  • Paid holidays and paid time off
  • A welcoming work environment

The Role

We are seeking an experienced Clinical Research Coordinator/Clinical Research Coordinator III for our Artemis Institute of Research clinical trial site located in Riverside, California. Under the supervision of the Site Director, the Senior Clinical Research Coordinator is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines. The Senior Clinical Research Coordinator manages study conduct from planning through study closeout.

Position Type:  Full Time

Pay Range:  $76,000-$90,000/yr

Location:  Riverside, CA

Work Schedule: Monday through Friday, 9:30am-6:00pm

Responsibilities:

  • In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality
  • Managing all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending investigator meetings
  • Experience managing multiple studies as the primary coordinator and someone ready to take the next step in managing people
  • Providing the highest level of care for study patients and delivering excellent customer service to the pharmaceutical clients

Qualifications:

  • Nursing license, medical assistant certificate or registration preferred
  • Minimum of two years of experience as a designated Clinical Research Coordinator on clinical trials required; sponsor-initiated and pharma clinical trials preferred
  • Previous clinical experience in a hands-on patient-facing role required
  • Commitment and ability to deliver excellent customer service
  • Excellent communication, punctual and responsible
  • Extremely well organized
  • Excellent verbal and written communication skills
  • Trustworthy, reliable; attentive to details
  • Mature and pleasant demeanor
  • Willingness to learn new tasks and grow with the company

Apply