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Clinical Research Program Manager Jobs in Riverside, CA

Kelly Services

Clinical Research Specialist

Irvine, CA · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

May serve as the primary contact for clinical trial sites (e.g. site management); * Assists in the ... Ability to travel approximately 20% depending on the phase of the program. As part of our promise ...

Kelly Services

Clinical Research Specialist

Irvine, CA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This person will join our Kelly FSP (Functional Service Provider) division, a managed solution ... Clinical Research Specialist DUTIES & RESPONSIBILITIES Under general direction and in accordance ...

Jj

Principal Clinical Research Scientist

Irvine, CA

  • Medical

  • Vision

  • Life

  • Retirement

  • PTO

Experience supporting product development and lifecycle management Clinical Research Leadership * Led clinical studies or clinical programs, not just participated in them * Experience designing ...

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All JobsClinical Research Program JobsClinical Research Program Manager JobsClinical Research Program Manager Jobs in Riverside, CA

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 Aug 15, 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 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 the key skills and qualifications needed to thrive as a clinical research program manager?

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 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

Dietitian / Clinical Research Coordinator

Irvine Clinical Research

Riverside, CA

$30 - $40/hr

Full-time

Medical, Dental, Vision, PTO

Re-posted 17 days ago

Job description

Irvine Clinical Research is the largest independent clinical trial group on the West Coast. We're expanding our research in GLP-1 and incretins, testing the efficacy and safety of investigational anti-obesity medications. Can these drugs help participants manage their weight, reduce their risk of developing obesity-related complications, or even help with conditions such as depression?
 
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while coordinating clinical trials. Your work may contribute to the advancement of truly life-changing treatments.
Job Duties
  • Conduct lifestyle counseling visits to improve nutrition and dietary quality, mental health/coping skills, and health behavior habits
  • Manage daily operations for assigned clinical trial projects
  • Perform study procedures in accordance with GCP and study protocols
  • Organize and maintain paper and electronic study data in a complete and correct manner
  • Cultivate enthusiastic and professional relationships with study participants and sponsors alike
  • Work closely with recruitment and prescreening teams to meet study enrollment goals
  • Conduct diagnostic, efficacy, and safety assessments as needed
Job Qualifications
  • Bachelor's or graduate degree from an accredited dietetics program
  • Valid Registered Dietitian (RD) or Registered Dietitian Nutritionist (RDN) Certification
  • Attention to detail and the ability to handle multiple tasks with precision
  • A command of professional spoken and written English
  • One (1) or more years of clinical research experience
$30 - $40 an hour
Hours and Compensation
This is a partial full time (30 hours/week) employment position based in-person in Long Beach, Irvine, or Riverside on Mon-Thu 8:00a-4:00p.
 
The starting salary for this position is $30/hour. Higher salary is negotiable with candidates who have more experience with pharmaceutical clinical trials.
 
The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees. Vacation (PTO) for this role will be earned at a rate of 11.25 days per year.
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