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Clinical Research Program Manager Jobs in Riverside, CA

Medix

Clinical Research Coordinator

Murrieta, CA · On-site

$31 - $38/hr

Additional duties as assigned by management. Required Skills * Must have oncology clinical research experience * Minimum of two years of clinical research experience Preferred Skills * Bachelor ...

Flourish Research

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

... management Requirements * Bachelor's degree preferred, but not required * Clinical research ... leave, referral program, employee assistance program, life insurance, disability insurance ...

Flourish Research

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

... management Requirements * Bachelor's degree preferred, but not required * Clinical research ... leave, referral program, employee assistance program, life insurance, disability insurance ...

Flourish Research

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

... management Requirements * Bachelor's degree preferred, but not required * Clinical research ... leave, referral program, employee assistance program, life insurance, disability insurance ...

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Track and manage trial documentation, including but not limited to site contracts, investigator ...

Diality Inc

Clinical Research Associate

Irvine, CA · On-site

$120K - $135K/yr

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Track and manage trial documentation, including but not limited to site contracts, investigator ...

Masimo Corporation

Clinical Research Lab RN II

Irvine, CA · On-site

$55 - $72/hr

Ability to independently set and manage multiple priorities * Demonstrates advanced judgment and ... Employee Assistance Program * Pet Insurance * on-site Wellness Clinic * Fitness Center * Café All ...

Masimo

Clinical Research Lab RN II

Irvine, CA · On-site

$40 - $52/hr

Ability to independently set and manage multiple priorities * Demonstrates advanced judgment and ... Program, Pet Insurance, on-site Wellness Clinic, Fitness Center, Cafe. All benefits are subject to ...

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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 Sep 5, 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 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 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 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 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

Regulatory Research Assistant - (Clinical Research)

CenExel CIT

Riverside, CA • On-site

$20 - $22/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 4 days ago

Job description

About Us:
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Hourly Rate: $20.00 - $22.00/hour (depending on education, experience, and skillset)
Schedule: Monday - Friday 08:00 AM - 04:30 PM
Job Summary:
Assist the Regulatory Specialists/Manager in maintaining clinical trial documents for submission to regulatory agencies in accordance to site SOPs, ICH, GCP, and FDA guidelines.
SOPs (Standard Operating Procedures)
ICH (International Council for Harmonization)
GCP (Good Clinical Practices)
FDA (Food and Drug Administration)
Essential Responsibilities and Duties:
  • Complies with current protocols, site SOPs, GCPs, IRB (Institutional Review Board) and FDA guidelines.
  • Uploads regulatory documents with RealTime eDOCs System and files is paper binders, as necessary.
  • Prepares, obtains, organizes and maintains regulatory and training documents in various storage mediums.
  • Tracks submissions and ensure timely filing of documents.
  • Obtains CVs (Curriculum Vitae) of external Investigators and other contract personnel and their signatures for appropriate regulatory documents.
  • Forwards revised copies of protocols, informed consents, and other pertinent study documents to appropriate staff.
  • Assists in obtaining necessary signatures from investigators.
  • Works closely with study sponsor/CRO and key clinical trial personnel on relevant regulatory document issues.
  • Ensures Clinical Conductor regulatory information is current.
  • Participates in team meetings and complies with training requirements.
  • Assists sponsors/CRO's as needed.
  • Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
  • 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.

Education/Experience/Skills:
  • Must be able to effectively communicate verbally and in writing.
  • Minimum: High School graduate or equivalent.
  • Minimum of 1 year of related experience in clinical research
  • Must be self-directed and able to work with minimal supervision.
  • Able to take a flexible approach to shifting priorities.
  • Motivated to work consistently in a fast-paced and rapidly changing environment.

Working Conditions
  1. Indoor, Office environment.
  2. Essential physical requirements include sitting, typing, standing, and walking.
  3. Lightly active position, occasional lifting of up to 20 pounds.
  4. Reporting to work, as scheduled, is essential.
  5. Ability to work overtime, weekends, and/or holidays as needed.
  6. Ability to travel as needed.
  7. Remote work arrangement depending on location.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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