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

Jj

Clinical Research Leader

Irvine, CA · On-site +1

May serve as the primary contact for clinical trial sites (e.g. site management); * Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual ...

Johnson and Johnson

Clinical Research Leader

Irvine, CA · On-site +1

May serve as the primary contact for clinical trial sites (e.g. site management); * Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual ...

Johnson & Johnson

Clinical Research Leader

Irvine, CA · On-site +1

May serve as the primary contact for clinical trial sites (e.g. site management); * Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual ...

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

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$30

$65

$100

How much do clinical trial manager jobs pay per hour?

As of Sep 2, 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 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 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 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.

How much does a clinical trial manager earn?

A clinical trial manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory requirements and project management tools.

What qualifications do you need to be a clinical trial manager?

A clinical trial manager typically needs a bachelor's degree in life sciences, healthcare, or a related field, along with experience in clinical research or project management. Many roles also require knowledge of Good Clinical Practice (GCP) guidelines and proficiency with trial management software. Advanced degrees or certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.
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Clinical Trial Manager jobs near you
Infographic showing various Clinical Trial Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 82% Full Time, 17% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $135,661 per year, or $65.2 per hour.

Obesity Medicine Specialist (Clinical Trial Physician) - Pomona, CA

ProTouch Staffing

Pomona, CA

$100 - $200/hr

Other

Re-posted 3 days ago

Job description

Obesity Medicine Specialist (Clinical Trial Physician) - Pomona, CA
Job Type: Part-Time
Shift: Day

Position Summary:
We are seeking a board-certified Obesity Medicine Specialist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I). The physician will oversee patient safety, ensure protocol compliance, and work closely with research staff to deliver high-quality trial outcomes.
Key Responsibilities:
  • Serve as PI or Sub-I on assigned obesity medicine clinical trials.
  • Conduct participant evaluations, medical exams, and determine eligibility.
  • Monitor patient safety, adverse events, and treatment outcomes.
  • Review and approve study-related documentation per protocol and regulations.
  • Collaborate with coordinators, nurses, and research staff.
  • Participate in protocol training and maintain compliance with GCP standards.
Qualifications:
  • MD or DO with an active State medical license.
  • Board-certified in Obesity Medicine or Endocrinology.
  • Prior clinical research experience preferred (training provided if needed).
  • Strong organizational, communication, and teamwork skills.
Compensation & Benefits:
  • $100-$200 per hour (depending on study complexity).
  • Flexible schedule: 0-8 hours/week.
  • Professional growth opportunities in clinical research.
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About Protouch Staffing

Sourced by ZipRecruiter

Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Frisco, TX, US

Year founded

1989

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