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Clinical Research Program Manager Jobs in Riverside, CA

JenaValve

Manager, Clinical Research Affairs

Irvine, CA · On-site

$145K/yr

Manager, Clinical Research Affairs Role Level: People Manager Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA - Corporate office environment Summary: The ...

JenaValve

Senior Associate, Clinical Research

Irvine, CA · On-site

$95K/yr

Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The Senior Clinical Research Associate will report ...

Masimo

Clinical Research Data Scientist (RWE)

Irvine, CA · On-site

... programs and regulatory submissions. The Clinical Research Data Scientist- Real World Evidence (RWE ... Data Science, Analytics and Management * Apply advanced statistical methods to large-scale datasets ...

Jj

Staff Clinical Research Scientist

Irvine, CA

Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting ... This role is responsible for writing and managing manuscripts, abstracts, posters, and ...

Masimo

Clinical Research Data Scientist (RWE)

Irvine, CA · On-site

... programs and regulatory submissions. The Clinical Research Data Scientist- Real World Evidence (RWE ... Data Science, Analytics and Management * Apply advanced statistical methods to large-scale datasets ...

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All 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 Jul 4, 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, 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 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
Clinical Research Operations Specialist

Clinical Research Operations Specialist

Loma Linda University Health

Loma Linda, CA

Other

Posted 18 days ago

Loma Linda University Health rating

8.2

Company rating: 8.2 out of 10

Based on 87 frontline employees who took The Breakroom Quiz

109th of 1,004 rated hospitals

Job description

MC: Cancer Institute Core- Temporary- Full-Time, Day Shift

Job Summary: The Clinical Research Operations Specialist for the Cancer Center Clinical Trials Unit (CCCTU) plays a critical role in the financial management of clinical research trials from study startup to study closure.  The Clinical Research Operations Specialist participates in the start-up activities related to opening new trials, including performing financial feasibility assessments, and will work closely with the Principal Investigator, study start-up team and Research Affairs Financial Management to ensure accurate and compliant budget development and negotiation.   Develops the Medicare Coverage Analysis to begin budget development. Creates new studies in the OnCore Clinical Trial Management System and tract contract milestones and EPIC to support charge review and research billing compliance.  The Clinical Research Operations Specialist develops and negotiates budgets for clinical trials working with sponsors, ancillary departments, and billing offices.  This position requires the ability to interpret study protocols, identify billable vs research-only procedures and ensure alignment between clinical activities and financial workflows.  Facilitates and processes financial transactions for clinical trial accounts.   Performs other duties as needed. 

Education and Experience: Bachelor's Degree in Healthcare Administration, Finance, or account required.   Minimum two years experience in clinical research finance, budget development or contract negotiation required.  Experience with oncology clinical trials at an academic medical center or cancer research institution preferred.    

Knowledge and Skills: Knowledge of clinical trial practices, billing compliance regulation, Medical coverage analysis, and medical terminology.   Familiarity with budgeting for cell therapy studies. Experience with early phase or complex trial designs.  Knowledge of fair market value standards and budgeting practices for high-cost research procedures.  Working knowledge of CPT codes, RVUs, and Medicare billing practices in clinical research.  Read, write legibly, and speak in English with professional quality; use computer, printer, and software programs necessary to the position (e.g., Word, Excel, Outlook, PowerPoint). Operate/troubleshoot basic office equipment required for the position.  Relate and communicate positively, effectively, and professionally with others; work calmly and respond courteously when under pressure; collaborate and accept direction.  Think critically; manage multiple assignments effectively; organize and prioritize workload; work well under pressure; problem solve; recall information with accuracy; pay close attention to detail; work independently with minimal supervision.  Distinguish colors as necessary; hear sufficiently for general conversation in person and on the telephone, and identify and distinguish various sounds associated with the workplace; see adequately to read computer screens, and written documents necessary to the position.

Licensures and Certifications: None.

Our mission is to continue the teaching and healing ministry of Jesus Christ. Our core values are compassion, excellence, humility, integrity, justice, teamwork and wholeness.
Loma Linda University Health is a Seventh-day Adventist, faith and values based Christian institution. Candidates must understand and embrace the mission, purpose, and identity of Loma Linda and its affiliated entities.

We are an equal opportunity employer committed to the principles of diversity. We provide equal opportunities in all aspects of the employment process to every individual, regardless of gender, race, color, age, national origin, ancestry, physical or mental disability, marital or veteran status, genetic information or any other characteristic protected by law. In addition, we will provide reasonable accommodations for otherwise qualified individuals requesting an accommodation due to a disability. If you need accommodation assistance with accessing our job listings or completing an application, or during any other phase of employment with us, please contact Human Resources Management at (909) 651-4001.

Loma Linda University Medical Center is a religiously-qualified Equal Opportunity Employer under Title VII of Civil Rights Act of 1964. No question on this application is asked for the purpose of unlawfully limiting or excluding any applicant's consideration for employment because of race, color, religion, gender, age, national origin, disability, genetic information, or any other status protected by applicable law. If you need a reasonable accommodation in the hiring process, please notify Human Resource Management.

We appreciate your interest in Loma Linda and wish you success in your job search!

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About Loma Linda University Health

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Loma Linda University Health (LLUH) is an esteemed healthcare organization situated in Loma Linda, California, US. Established in 1905, it was initially known as the College of Medical Evangelists, and it operated as the official medical institution of the Seventh-day Adventist Church until the name was changed to LLUH in 1961. LLUH is very much active in the healthcare and education sectors, providing a vast range of services such as medical treatment, research, and health education. The organization’s core mission is "to continue the teaching and healing ministry of Jesus Christ", which underlines its binding values of compassion, integrity, excellence, freedom, and justice.

Industry

Health care and social assistance and hospitality services

Company size

10,000+ Employees

Headquarters location

Loma Linda, CA, US

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