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Clinical Research Project Manager Jobs in Riverside, CA

Jj

Clinical Research Leader

Irvine, CA · On-site +1

Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting ... Supports planning, track and manage assigned project budgets to ensure adherence to business plans;

Johnson & Johnson

Clinical Research Leader

Irvine, CA · On-site +1

Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting ... Supports planning, track and manage assigned project budgets to ensure adherence to business plans;

Jj

Staff Clinical Research Scientist

Irvine, CA

Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting ... Strong project management skills to balance multiple projects * Excellent interpersonal skills ...

Azul Vision

Clinical Research Coordinator

Redlands, CA

$21 - $27/hr

The Clinical Research Coordinator works closely with pharmaceutical companies, assisting principal ... Manage and ensure completion of all study start-up documents for proper documentation and ...

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All 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 4, 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
Senior Clinical Research Coordinator

Senior Clinical Research Coordinator

Headlands Research

Riverside, CA • On-site

$76K - $90K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

Job description

Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more than 50 years of combined research experience, Artemis specializes in Psychiatry/Neurology, Internal Medicine, and Women's Health studies. With multiple locations serving Southern California, including San Diego and Riverside, each Artemis site is fully equipped to conduct complex clinical research trials. 

Want to be a part of a growing company that's making a difference in our world? Look no further than Artemis Institute for Clinical Research! You'll enjoy a friendly and exciting culture with opportunities for growth and advancement. We offer the following generous benefits to our full-time employees:

  • A range of PPO and HMO medical plans
  • PPO and HMO dental plans
  • Vision coverage, long term disability plan, and life/AD&D coverage
  • 401k plan
  • Paid holidays and paid time off
  • A welcoming work environment

The Role

We are seeking an experienced Clinical Research Coordinator/Clinical Research Coordinator III for our Artemis Institute of Research clinical trial site located in Riverside, California. Under the supervision of the Site Director, the Senior Clinical Research Coordinator is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines. The Senior Clinical Research Coordinator manages study conduct from planning through study closeout.

Position Type:  Full Time

Pay Range:  $76,000-$90,000/yr

Location:  Riverside, CA

Work Schedule: Monday through Friday, 9:30am-6:00pm

Responsibilities:

  • In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality
  • Managing all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending investigator meetings
  • Experience managing multiple studies as the primary coordinator and someone ready to take the next step in managing people
  • Providing the highest level of care for study patients and delivering excellent customer service to the pharmaceutical clients

Qualifications:

  • Nursing license, medical assistant certificate or registration preferred
  • Minimum of two years of experience as a designated Clinical Research Coordinator on clinical trials required; sponsor-initiated and pharma clinical trials preferred
  • Previous clinical experience in a hands-on patient-facing role required
  • Commitment and ability to deliver excellent customer service
  • Excellent communication, punctual and responsible
  • Extremely well organized
  • Excellent verbal and written communication skills
  • Trustworthy, reliable; attentive to details
  • Mature and pleasant demeanor
  • Willingness to learn new tasks and grow with the company

Apply