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

JenaValve

Specialist, Clinical Safety

Irvine, CA · On-site

$100K/yr

Experience with EDC (Electronic Data Capture) platforms for clinical trial management and safety reporting. * Basic understanding of clinical trial design and statistical concepts as applied to ...

Kaygen Inc.

Spec 3, Clinical Research

Irvine, CA · On-site

This role is responsible for organizing, reviewing, and maintaining clinical documentation within the Electronic Trial Master File (eTMF) and Clinical Trial Management System (CTMS) to ensure ...

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Track and manage trial documentation, including but not limited to site contracts, investigator ...

Diality Inc

Clinical Research Associate

Irvine, CA · On-site

$120K - $135K/yr

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Track and manage trial documentation, including but not limited to site contracts, investigator ...

Kaygen

Spec 3, Clinical Research

Irvine, CA · On-site

This role is responsible for organizing, reviewing, and maintaining clinical documentation within the Electronic Trial Master File (eTMF) and Clinical Trial Management System (CTMS) to ensure ...

City of Hope

Clinical Study Coord

Irvine, CA

Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...

City of Hope

Clinical Study Coord

Irvine, CA · On-site

Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...

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 ...

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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.

Clinical Research Specialist 3

Kaygen Inc.

Irvine, CA • On-site

Other

Posted 27 days ago

Job description

Job Title: Clinical Research Specialist Location: Irvine, CA Duration: 6 Months Job Description: Job Description - The main function of the Clinical Research Specialist is to support clinical study start‐up, execution, and closeout with a strong emphasis on maintaining an inspection‐ready Trial Master File (TMF). Responsibilities include organizing, reviewing, and quality‐checking essential documents in the eTMF and CTMS to ensure compliance with GCP, regulatory requirements, and internal SOPs. The Specialist identifies and investigates documentation discrepancies, supports data review and query resolution with cross‐functional teams, and contributes to process improvements that enhance efficiency and documentation quality across clinical studies. Key Responsibilities: Participate in study start-up activities (e.g., tracking site readiness, communication with clinical trial sites about planning and logistics of site qualification visit and site initiation visit, and other associated supporting tasks), as well as study execution and closure activities. Organize and manage documents in the Electronic Trial Master File (eTMF) and Clinical Trial Management System (CTMS) to ensure compliance with internal procedures. Review clinical data for completeness across multiple research trials and conduct thorough documentation reviews for internal and external audits (e.g., FDA, TUV, PMDA) to ensure all essential Trial Master File (TMF) documents adhere to Good Documentation Practices, Edwards' internal SOPs, and relevant US and OUS regulations. Review, identify and investigate discrepancies in study documentation by applying clinical protocol and GCP knowledge and develop processes to mitigate reoccurrence throughout study conduct and closeout Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution Supports assessments of current processes, identifies opportunities and assists with improving process efficiency within and across related functional areas Education and Experience Requirements: Bachelor's Degree or equivalent in related field 1-2 year of clinical research experience required Additional Skills (Preferred): Good computer skills in usage of MS Office Suite and Clinical Systems such as CTMS (Clinical Trial Management System), eTMF (electronic Trial Master file) preferred. Good written and verbal communication skills and interpersonal relationship skills Good problem-solving and critical thinking skills Good understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting Strict attention to detail Ability to manage competing priorities in a fast paced environment Must be able to work in a team environment, including immediate supervisor and other team members in the section or group

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