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Clinical Research Project Manager Jobs in Riverside, CA

Kelly Services

Clinical Research Specialist

Irvine, CA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Clinical Research Specialist DUTIES & RESPONSIBILITIES Under general direction and in accordance ... management level. Function as a reliable, trusted resource of accurate, up-to-date project ...

Jj

Principal Clinical Research Scientist

Irvine, CA · On-site

  • Medical

  • Vision

  • Life

  • Retirement

  • PTO

Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting ... and Project Management partners to deliver on time, within budget, and in compliance with ...

New

Flourish Research

Clinical Research Coordinator

Murrieta, CA

$31 - $38/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Additional duties as assigned by management. Requirements * Bachelor's degree preferred, but not required * Must have oncology clinical research experience * Minimum of two years of clinical research ...

Flourish Research

Clinical Research Coordinator

Murrieta, CA · On-site

$31 - $38/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Additional duties as assigned by management. Requirements * Bachelor's degree preferred, but not required * Must have oncology clinical research experience * Minimum of two years of clinical research ...

Flourish Research

Clinical Research Coordinator

Murrieta, CA · On-site

$31 - $38/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Additional duties as assigned by management. Requirements * Bachelor's degree preferred, but not required * Must have oncology clinical research experience * Minimum of two years of clinical research ...

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Showing results 21-40

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 Aug 15, 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?

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 August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $89,754 per year, or $43.2 per hour.

Clinical Research Specialist

Kelly Services

Irvine, CA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 13 days ago

Job description

Kelly Science and Clinical FSP is currently seeking a Clinical Research Specialist for a long-term engagement in Irvine, CA with one of our Global Medical Device clients. This position is hybrid. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
Clinical Research Specialist
DUTIES & RESPONSIBILITIES
Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate, procedures and guidelines, this position
  • Serves as a Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestone
  • Participates in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedure
  • May serve as the primary contact for clinical trial sites (e.g. site management
  • Assists in the development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports
  • Supports applicable trial registration (e.g. www.clinicaltrials.gov) from study initiation through posting of results and support publications as needed
  • Coordinates and executes ordering, tracking, and accountability of investigational devices and trial materials
  • Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel
  • Interfaces and collaborates with Clinical Research Associates (CRAs)
  • Assists in overseeing and supports the development and execution of Investigator agreements and trial payments
  • Assists in clinical data review to prepare data for statistical analyses and publications
  • May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study needs
  • May provide on-site procedural protocol compliance and data collection support to the clinical trial sites
  • Assists in tracking assigned project budgets
  • May perform other duties assigned as needed
  • Responsible for communicating business related issues or opportunities to next management level. Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
  • Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures
  • Should develop a strong understanding of the pipeline, product portfolio and business needs
  • Generally, manages work with supervision. Independent decision-making for simple situations but requires guidance for complex situations
EXPERIENCE AND EDUCATION
Education:
  • Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science require
Experience:
  • BS with at least 2 years, MS and PhD with at least 1 year of relevant experience preferred
  • Previous experience in clinical research or equivalent is desired
  • Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR, MEDDEV,…)
  • Clinical/medical background is a plus
  • Medical device experience is a plus
REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS: Functional and Technical Competencies:
  • Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations
  • Proven track record in supporting clinical projects within clinical/ surgical research setting, on time, and in compliance to SOPs and regulations
  • Presentation and technical writing skills
  • Written and oral English communication skills

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.