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

AbbVie

Study Project Manager II

Irvine, CA

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager II ...

AbbVie

Study Project Manager II

Irvine, CA · On-site

$124K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager II ...

AbbVie

Study Project Manager II

Irvine, CA

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager II ...

City of Hope

Clinical Study Coord

Irvine, CA

Clinical Study Coordinator Join the transformative team at City of Hope, where we're changing lives ... Responsibilities include patient recruitment, informed consent, trial coordination, data management ...

City of Hope

Clinical Study Coord

Irvine, CA

Clinical Study Coordinator Join the transformative team at City of Hope, where we're changing lives ... Responsibilities include patient recruitment, informed consent, trial coordination, data management ...

CYNET SYSTEMS

Spec, Clinical Research

Irvine, CA · On-site

$48 - $53/hr

... study specific essential document lists, managing and communicating the status of study progress ... Identify and investigate discrepancies in study documentation by applying clinical protocol and GCP ...

Jj

Principal Clinical Research Scientist

Irvine, CA

  • Medical

  • Vision

  • Life

  • Retirement

  • PTO

Experience supporting product development and lifecycle management Clinical Research Leadership * Led clinical studies or clinical programs, not just participated in them * Experience designing ...

New

Jj

Senior Clinical Research Scientist

Irvine, CA · Hybrid

  • PTO

Manage with supervision clinical trials including study budget assessment, fair mark value appraisal, contract development and execution, payments, and development of study related materials * Ensure ...

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

Clinical Study Manager information

See Riverside, CA salary details

$30

$65

$100

How much do clinical study manager jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical study 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 are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

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

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

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

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

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

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

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 74% Full Time, 13% Part Time, and 13% Contract. Highlights an 100% In-person job distribution, with an average salary of $135,661 per year, or $65.2 per hour.

Clinical Study Administrator

Motion Recruitment Partners, LLC

Irvine, CA • On-site

Other

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

New

Job description

Kelly Science and Clinical FSP is currently seeking a Clinical Study Administrator for a long-term engagement with one of our Global MedTech clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
Job Description
Position Title: Clinical Study Administrator
Division: Clinical Operations
Reports To: Study Team Lead
Job Function Summary Overview:
This individual will provide support to the clinical study staff within Clinical Operations
Perform a variety of clinical research operations duties of a routine and technical nature in support of clinical trials.
Supports project managers within the assigned clinical studies.
Key Job Activities: Under direction of Clinical Operations personnel, and in accordance with all applicable Regional, state and local laws/regulations and corporate procedures and guidelines, this position will
  • As directed, provides support to the project teams which may include tracking study data, following-up with clinical sites on essential documents; assist in drafting and distributing study mailings, including study newsletters; assist in drafting of agenda/meeting minutes and scheduling of meetings.
  • Assist in payments/tracking for patient reimbursements.
  • Performs data entry in systems
  • Run reports including training matrix reports, metrics for management reviews
  • Support management of IRB/IEC renewal compliance.
  • Coordinate process for the review of study data, such as MRIs, by third-party vendors.
  • Assist in ordering, shipping, tracking of, study supplies including, but not limited to, investigational devices and site binders. Maintain master device accountability log as requested.
  • Assist with scheduling and organizing investigators and expert panel meetings.
  • Assist with file reviews and Audit preparation
  • Is responsible for ensuring appropriate level of communication with managers, project leaders, and team members.
  • Work with management group to help achieve department goals.
  • Participate in process improvement activities within the department.
  • May be involved in other tasks to support Clinical Operations and Operating Company as needed.

Other Administrative Tasks
  • Know, understand, incorporate, and comply with all applicable laws and regulations relating to business activities and Policies and Procedures of the Health Care Compliance Program and Code of Conduct.
  • May be asked to provide additional support to Clinical Operations staff, as needed.
Job Qualifications
Education
  • Minimum of a Bachelor's Degree is required.

Experience
  • Previous clinical research experience
  • Requires previous administrative support experience or equivalent for at least 1 year.
  • Clinical/medical background

Knowledge
  • Requires experience and knowledge working with computer systems (Microsoft office - Excel, Word and Power Point).
Additional Requirements
  • Demonstrated competencies in the following areas are required:
    • Tracking
    • Written and verbal communications
    • Attention to details
    • Organizational skills

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