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Clinical Trials Jobs in Riverside, CA (NOW HIRING)

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Clinical Trials information

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$65

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How much do clinical trials jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical trials in Riverside, CA is $65.22, according to ZipRecruiter salary data. Most workers in this role earn between $52.93 and $73.46 per hour, depending on experience, location, and employer.

What is a clinical trial?

A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

What are some common career paths or advancement opportunities for professionals working in clinical trials?

Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.

What are the key skills and qualifications needed to thrive in a clinical trials position, and why are they important?

To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.

What are the most commonly searched types of Clinical Trials jobs in Riverside, CA?

The most popular types of Clinical Trials jobs in Riverside, CA are:

What are popular job titles related to Clinical Trials jobs in Riverside, CA?

For Clinical Trials jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Clinical Trials jobs in Riverside, CA look for?

The top searched job categories for Clinical Trials jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Clinical Trials jobs?

Cities near Riverside, CA with the most Clinical Trials job openings:

Clinical Trials jobs near you
Infographic showing various Clinical Trials job openings in Riverside, CA as of September 2026, with employment types broken down into 2% As Needed, 74% Full Time, 18% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $135,661 per year, or $65.2 per hour.

Clinical Trials Operations Lead

Irvine, CA • On-site

Kelly Science, Engineering, Technology & Telecom
See more jobs at Kelly Science, Engineering, Technology & Telecomexternal

Other

Posted 2 days ago

New

Job description

  • Serves as a Clinical Research Specialist within the Clinical R&D Operations CoE operations group to execute company sponsored clinical trials for the Medical Device division
  • Serves as a member of the clinical trial/study core team and may serve as the liaison with the Clinical R&D Franchise and Clinical R&D BSDM for projects under his/her responsibility
  • May serve as the primary contact for clinical trial sites
  • Manage operational activities of assigned clinical studies within the Clinical R&D Operations group
  • Solves problems with support from Clinical Management arising during clinical trial execution
  • Provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
  • May be involved in other tasks to support Clinical R&D Operations and R&D Clinical Franchise as needed
  • Track assigned projects budgets to ensure adherence to business plans
  • Support the implementation of new clinical systems/processes, and provide support for publications, as needed.
  • Interface and collaborate with site personnel, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel
  • Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance
  • Ensure efficient use of resources within the clinical study/program to provide high quality deliverables.

Business Leadership Responsibilities:

  • Accountable for quality, compliance with regulations and company procedures, timelines, and budgets for assigned clinical trials.
  • May lead several non-regulated small clinical trials and/or a small number of non-regulated medium trials that may involve other clinical operations staff.
  • May assist with the management of large regulated or complex trials under supervision of CTM or Senior CTM.
  • Identify and ensure strategies, resources, and accountabilities are in place to achieve rapid, high quality execution of assigned clinical trials under his/her responsibilities.

Qualifications:

  • Minimum of a Bachelor’s/University Degree or equivalent required; preferably in Life Science, Physical Science, Nursing, or Biological Science.
  • 2-4 years of relevant experience (or equivalent) required.
  • Previous experience in clinical trial management or equivalent is desired.
  • Relevant industry certifications preferred (i.e., CCRA, RAC, CDE).
  • Clinical/medical background a plus.
  • Requires understanding of Good Clinical Practices
  • Understanding and application of regulations and standards applied in clinical areas/regions is required
  • Presentation skills and influencing of others
  • Written and oral communication skills
  • Demonstrated competencies in the following areas are required: Behaving in a professional and ethical manner
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