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Clinical Research Program Manager Jobs in Riverside, CA

Wake Research

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 ...

Flourish Research

Clinical Research Coordinator

Murrieta, CA · On-site

$31 - $43/hr

... program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 ... Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol ...

Flourish Research

Clinical Research Coordinator

Murrieta, CA · On-site

$31 - $43/hr

... program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 ... Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol ...

Jj

Clinical Research Manager

Irvine, CA · Hybrid

Clinical project leadership across multiple studies/ programs is required. * Experience working ... Research, Strategic Change, Study Management, Team Management The anticipated base pay range for ...

Johnson & Johnson

Clinical Research Manager

Irvine, CA · Hybrid

Clinical project leadership across multiple studies/ programs is required. * Experience working ... Research, Strategic Change, Study Management, Team Management The anticipated base pay range for ...

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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

Clinical Research Recruitment Coordinator

Irvine Clinical Research

Irvine, CA

$52K/yr

Full-time

Posted 4 days ago

Job description

Irvine Clinical Research is the largest independent memory research center on the West Coast.

Alzheimer's Disease is a serious cognitive illness that affects millions of people each year. Every research trial brings us closer to finding a treatment or cure for Alzheimer's Disease. A recent study conducted at Irvine Clinical Research was successful in slowing cognitive decline by as much as 27%.

Irvine Clinical Research is looking for a friendly, outgoing person to join our team as a Clinical Research Recruitment Coordinator. You will be speaking with potential study participants about their health concerns, especially around memory loss, and when appropriate, presenting research as a care option.
In this role, expect to
  • Recruit study participants via short telephone interviews; make outbound phone calls to achieve appointment scheduling goal
  • Build rapport with potential participants to ensure engagement and retention
  • Promote Irvine Clinical Research's services and the opportunity to advance the fight against Alzheimer's Disease via study participation
  • Work independently while still being accountable to recruitment goals
  • Input data into electronic systems in a consistently timely and accurate manner
  • Assist with other recruitment, marketing, and outreach efforts as needed
To succeed in this role, you have
  • A welcoming, friendly, and professional attitude and demeanor that you bring with you every day
  • Ability to consistently build trust and rapport with persons concerned about memory
  • High attention to detail for all of your work responsibilities
  • Time management skills to coordinate and manage recruitment calls efficiently 
Nice to have, but not essential
  • Experience speaking with people with cognitive issues or older adults
  • Call center or clinical research experience
  • Salesforce/CRM/CTMS experience
Hours and Compensation
This is a full-time employment position based in-person at our clinic in the Alzheimer’s Orange County building in Irvine. There is an opportunity to transition to hybrid or remote work after 6 consecutive months of meeting performance standards.

The starting salary for this position is $25 per hour (approximately $52k per year).

The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees. Vacation (PTO) is earned at a rate of 3 weeks per year.
Equal Employment Opportunity
Irvine Clinical Research is committed to diversity within our organization and building an equitable and inclusive environment for people of all backgrounds and experiences. Irvine Clinical Research provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, Irvine Clinical Research complies with all state and local laws governing nondiscrimination in employment in any location. We especially encourage members of traditionally underrepresented communities to apply, including women, people of color, LGBTQ people, veterans, and people with disabilities.