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Clinical Trial Manager Jobs in Riverside, CA (NOW HIRING)

JenaValve

Associate, Clinical Research

Irvine, CA · On-site

$75K/yr

Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current. * Conduct ...

Kelly Services

Clinical Research Specialist

Irvine, CA · On-site

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 ...

Kelly Services

Clinical Research Specialist

Irvine, CA · Hybrid

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 ...

Kelly Services

Clinical Research Specialist

Irvine, CA · Hybrid

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 ...

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All JobsClinical Trial JobsClinical Trial Manager JobsClinical Trial Manager Jobs in Riverside, CA

Clinical Trial Manager information

See Riverside, CA salary details

$30

$65

$100

How much do clinical trial manager jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical trial manager 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 does a clinical trial manager do?

A clinical trial manager, or CTM, oversees research and each phase of clinical drug tests at a hospital. They work closely with both the doctors and clinicians who are performing the trial, as well as the sponsor of the study, which is typically a pharmaceutical company or other health care organization. As a CTM, duties and responsibilities include planning and managing the trial, making sure that the test meets all government standards, and determining if it was successful. Clinical trial managers also hire, train, and evaluate the members of the clinical team.

What are the key skills and qualifications needed to thrive as a clinical trial manager, and why are they important?

To thrive as a Clinical Trial Manager, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's or master's degree. Familiarity with clinical trial management systems (CTMS), regulatory requirements like GCP, and certifications such as ACRP or SOCRA are highly beneficial. Strong organizational skills, attention to detail, leadership, and effective communication are critical soft skills for managing teams and stakeholders. These skills ensure trials are conducted ethically, efficiently, and compliantly, leading to successful study outcomes.

What does a clinical trial manager do?

A Clinical Trial Manager oversees the planning, coordination, and execution of clinical trials for new drugs, medical devices, or treatments. They ensure that trials are conducted in compliance with regulatory guidelines, company protocols, and ethical standards. Their responsibilities include managing budgets, timelines, and teams, as well as monitoring data quality and safety throughout the study. Clinical Trial Managers also work closely with investigators, sponsors, and regulatory agencies to ensure successful trial outcomes.

What are some common challenges clinical trial managers face when coordinating multi-site studies?

Clinical Trial Managers often encounter challenges such as ensuring consistent protocol implementation across different sites, managing timelines in the face of site-specific delays, and maintaining clear communication among diverse teams. They must also navigate regulatory differences between regions and address unforeseen issues like patient recruitment shortfalls or data discrepancies. Success in this role requires strong organizational skills, adaptability, and proactive problem-solving to keep studies on track and compliant.
More about Clinical Trial Manager jobs
What are the most commonly searched types of Clinical Trial jobs in Riverside, CA? The most popular types of Clinical Trial jobs in Riverside, CA are:
What are popular job titles related to Clinical Trial Manager jobs in Riverside, CA? For Clinical Trial Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Manager jobs in Riverside, CA look for? The top searched job categories for Clinical Trial Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Clinical Trial Manager jobs? Cities near Riverside, CA with the most Clinical Trial Manager job openings:
Clinical Trial Manager jobs near you
Infographic showing various Clinical Trial Manager job openings in Riverside, CA as of July 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $135,661 per year, or $65.2 per hour.

Associate, Clinical Research

JenaValve

Irvine, CA • On-site

$75K/yr

Full-time

Re-posted 13 days ago

Job description

Job Title: Associate, Clinical Research
Role Level: Individual Contributor (IC)
Supervisor/Manager Title: Director, Clinical Affairs
Job Location & Environment: Irvine, CA, Corporate Office
Job Description Summary: The Clinical Research Associate will report to the Director, Clinical Affairs, and will play a key role in proactively supporting the conduct of pre-market and or post-market clinical studies and ensure compliance with all regulatory requirements. The ideal candidate will have a thorough knowledge of Good Clinical Practices (GCP) and applicable regulations.
Job Responsibilities:
  • Support site management and interact with site coordinators, investigators, and field monitors in collecting data and resolving queries to meet the protocol requirements in a timely manner.
  • Ensure quality data management activities - i.e., data review, query generation and resolution. Generate status reports to clinical staff and management.
  • Maintain Trial Master Files and trackers for clinical trials.
  • Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current.
  • Conduct periodic audits of internal files to ensure compliance per site Institutional Review Board (IRB) and/or Ethics Committee (EC) policy (i.e. IRB continuing review approval period and expiration dates).
  • Provide clinical operational support during preparation for and conduct of all clinical audits and inspections.
  • Contribute to the development and implementation of departmental policies, standards, and process improvement initiatives.
  • Partner with management to manage external vendors, including ongoing supplier qualification.
  • Assist field clinical monitors in preparation for site training and monitoring visits
  • Support monitoring of sites on an as-needed basis.

Required Education and Experience:
  • At least 1 year of experience in clinical trial research is required (preferred in medical devices).
  • Advanced degree in a biological science / pharmacy/ nursing desired.

Skills and Abilities Required for This Job:
  • Proficient in clinical trial management and electronic data capture systems to document and record information.
  • Excellent communication skills (written and verbal English) so as to be able to build effective relationships with trial center staff and colleagues.
  • Some knowledge of GCPs governing the conduct of clinical trials, Medical Device Directive 93/42/EEC, ISO14155 and ICH guidelines.
  • Very organized and able to pay close attention to detail.
  • Team player with a willingness to help where needed and work with diverse people.

Physical Requirements
  • Ability to travel up to 20% time.

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