ZipRecruiter

Log In

1

Clinical Research Project Manager Jobs in Riverside, CA

Jj

Clinical Research Manager

Irvine, CA · Hybrid

Clinical Development & Research - Non-MD Job Category: People Leader All Job Posting Locations ... Plans, tracks and manages assigned monitoring project budgets to ensure adherence to business plans

Johnson & Johnson

Clinical Research Manager

Irvine, CA · Hybrid

Clinical Development & Research - Non-MD Job Category: People Leader All Job Posting Locations ... Plans, tracks and manages assigned monitoring project budgets to ensure adherence to business plans

Jj

Clinical Research Manager

Irvine, CA · On-site +1

Clinical Development & Research - Non-MD Job Category: People Leader All Job Posting Locations ... Plans, tracks and manages assigned project budgets to ensure adherence to business plans;

next page

Showing results 1-20

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

Clinical Research Project Manager information

See Riverside, CA salary details

$52.2K

$89.8K

$137.7K

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

As of Jul 25, 2026, the average yearly pay for clinical research project manager in Riverside, CA is $89,754.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,600.00 and $95,500.00 per year, depending on experience, location, and employer.

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

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, clinics, academic institutions

The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.

What does a Clinical Research Project Manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

What are some common challenges faced by Clinical Research Project Managers and how can they be addressed?

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

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

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.
What are the most commonly searched types of Clinical Research Project jobs in Riverside, CA? The most popular types of Clinical Research Project jobs in Riverside, CA are:
What are popular job titles related to Clinical Research Project Manager jobs in Riverside, CA? For Clinical Research Project Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Project Manager jobs in Riverside, CA look for? The top searched job categories for Clinical Research Project Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Clinical Research Project Manager jobs? Cities near Riverside, CA with the most Clinical Research Project Manager job openings:
Clinical Research Project Manager jobs near you
Infographic showing various Clinical Research Project Manager job openings in Riverside, CA as of July 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $89,754 per year, or $43.2 per hour.
Clinical Research Program Manager - Quality Outcome & Grant Writing

Clinical Research Program Manager - Quality Outcome & Grant Writing

Pacific Neuropsychiatric Specialists Inc

Irvine, CA • On-site

$90K - $120K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 15 days ago

Job description

Benefits:
  • Health insurance
  • Paid time off
  • Vision insurance
  • 401(k) matching
  • Dental insurance

Position Summary
We are seeking a Clinical Research Program Manager to help develop and support the clinical outcome research program in mental health and substance use at Pacific Neuropsychiatric Specialist (PNS). This position will work directly with the clinicians and data analysts to establish research infrastructure, manage regulatory processes, coordinate clinical outcomes research, and assist in preparing manuscripts and scholarly publications in mental health and substance use clinical care. 
The ideal candidate is organized, detail-oriented, and an excellent scientific writer with experience in clinical research administration. This role does not require independent grant writing or serving as a principal investigator but requires the ability to translate research concepts into well-organized protocols and publication-ready manuscript drafts and grants.
Primary Responsibilities
  • Establish and maintain research infrastructure for an independent outpatient psychiatry research program.
  • Prepare and manage Institutional Review Board (IRB) submissions, amendments, continuing reviews, and regulatory documentation.
  • Develop research protocols, informed consent documents, case report forms, and standard operating procedures.
  • Coordinate clinical outcomes research projects from study initiation through publication.
  • Perform literature reviews and summarize current scientific evidence.
  • Draft manuscripts, abstracts, white papers, and conference presentations under the direction of the Principal Investigator.
  • Organize references using citation management software (e.g., EndNote, Zotero, or Mendeley).
  • Assist with data organization, quality assurance, and preparation of tables and figures for publication.
  • Coordinate with statisticians, collaborators, and journal editorial offices as needed.
  • Maintain study files and ensure compliance with applicable regulatory and ethical requirements.
Minimum Qualifications
  • Master's degree (e.g., MPH, MS, MA, or related field).
  • At least 2 years of experience in clinical research, research administration, or clinical study coordination, especially in psychiatry
  • Experience preparing and managing IRB submissions.
  • Excellent scientific and grant writing and editing skills.
  • Strong organizational and project management abilities.
  • Proficiency with Microsoft Office and reference management software.
Preferred Qualifications
  • Experience conducting literature reviews and preparing manuscripts for peer-reviewed journals.
  • Experience in value-based care highly preferred
  • Familiarity with REDCap or other clinical research databases.
  • Experience with clinical outcomes research or behavioral health research.
  • Working knowledge of basic biostatistics and interpretation of clinical research findings.
Desired Attributes
  • Exceptional attention to detail.
  • Strong written and verbal communication skills.
  • Ability to manage multiple projects simultaneously.
  • Self-motivated with the ability to work independently.
  • Collaborative and interested in building a research program from the ground up.