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

Jj

Clinical Research Leader

Irvine, CA · On-site

Serves as the main contact for clinical trial sites (e.g. site management). * Develop clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual ...

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Clinical Trial Manager information

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$30

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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.

Sub-Investigator (NP or PA) - Long Beach

Irvine Clinical Research

Irvine, CA

$140K/yr

Full-time

Medical, Dental, Vision, PTO

Posted 5 days ago

Job description

Healthy Brain Clinic in Long Beach, CA is part of the Irvine Clinical Research site network, the largest of its kind on the West Coast. With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity medicine. Our largest area of research is in Alzheimer's Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer's Disease.
 
We are hiring a clinical investigator--either a Nurse Practitioner (NP) or Physician Assistant (PA)--to join our Healthy Brain Clinic / Long Beach team. The clinician will oversee and conduct clinical trials of some of the most promising drugs under investigation in Alzheimer's Disease treatment and prevention, driving clinical excellence at our growing Long Beach site.
Job Duties
  • Clinical Trial Execution: Oversee and conduct protocol-driven clinical trial visits as a Sub-Investigator, ensuring strict adherence to FDA regulations, GCP guidelines, and study protocols.
  • Participant Eligibility & Medical Oversight: Conduct physical and neurological examinations, medical history assessments, clinical intake evaluations, and diagnostic reviews to evaluate participant safety and study eligibility.  
  • IV Line Placement & Infusions: Directly insert peripheral IV lines, administer investigational intravenous medications, and manage participant care and monitoring throughout active infusion procedures.
  • Participant Safety & Event Management: Monitor study participant safety throughout trial participation, managing and reporting adverse events in a thorough and timely manner.
  • Collaborative Research Team: Partner closely with Principal Investigators, fellow Sub-Investigators, clinical research coordinators, and study raters to ensure quality trial delivery.
Job Requirements
  • Licensure: Active, unencumbered license to practice as a Nurse Practitioner (NP) or Physician Assistant (PA-C) in California.
  • Clinical Skills: Demonstrated proficiency and hands-on skill in IV placement and intravenous infusions.
  • Patient Population: Clinical experience working with older adult populations in a primary care, specialty, or clinical research environment.
  • Research Experience: Prior experience as a Sub-Investigator or Clinical Research Coordinator in pharmaceutical industry trials is preferred, but not required.
  • Communication & Precision: Professional command of written and spoken English, with strong clinical documentation skills and a compassionate patient-facing demeanor.
$125,000 - $140,000 a year

  • Schedule & Hours: Full-time or part-time (minimum 20 hours per week). All hours are during normal weekday business hours with no planned overnight or weekend shifts.

  • Location: On-site at our Healthy Brain Clinic location in Long Beach: 1703 Termino Ave, Ste 201, Long Beach, CA 90804. Located in a modern medical building near the Traffic Circle with ocean views, convenient transit/freeway access, and ample free parking.

  • Network Integration: While anchored at our Long Beach site, opportunities for cross-coverage, regional investigator training, or multi-site trial support across our California network may be available.

  • Salary Range: $125,000/yr ($60.00/hr) to $140,000/yr ($67.31/hr). Placement within the range is based on experience, with higher starting compensation reserved for experienced Sub-Investigators in CNS, neurology, or psychiatry clinical trials.

  • Insurance: The company covers 100% of employee-only individual premiums for our baseline Gold HMO health plan, plus dental and vision coverage for eligible full-time staff.

  • Paid Time Off: 3 weeks of paid vacation (PTO) per year, plus paid sick leave and company holidays.

Equal Opportunity Employer

Healthy Brain Clinic and its affiliates are Equal Opportunity Employers. We evaluate all qualified applicants without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, gender identity, or any other status protected by CA state or federal law.

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