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Assistant Clinical Project Manager Jobs in Riverside, CA

Collabera

Clinical Data Manager

Irvine, CA · On-site

Clinical Data Manager Location: Irvine, CA USA 92618 Duration: 12 months (Strong Possibility of ... Labs, etc. Assist in overall project tasks such as process flowcharts, Standard Operating ...

AbbVie

Study Project Manager II

Irvine, CA · On-site

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 ...

New Behavior Transitions

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Assistant Clinical Director

San Bernardino, CA · On-site

$90K - $110K/yr

... care. * Assist with staff hiring, onboarding, training, and professional development while ... Support caseload management, scheduling, and clinical quality assurance initiatives to promote ...

AbbVie

Study Project Manager II

Irvine, CA · On-site

$124K/yr

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 Hesperia

Assistant Project Manager

Hesperia, CA · On-site

$7.9K - $9.7K/mo

Join the City of Hesperia's Engineering Department as an Assistant Project Manager and be part of a team driven by service, integrity, innovation, and efficiency. Help us create a safe, thriving ...

AbbVie

Study Project Manager II

Irvine, CA

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 ...

Hodess

Assistant Project Manager

Irvine, CA · On-site

$85K - $105K/yr

The Assistant Project Manager is pivotal in coordinating resources, communicating with stakeholders and monitoring project progress through completion. MAJOR AREAS OF RESPONSIBILITIES Project ...

Griffith Company

Assistant Project Manager

Brea, CA · On-site

$105K - $125K/yr

We are looking for an Assistant Project Manager to join our Landscape Division. This position is responsible for assisting the Project Manager in providing overall administrative and technical ...

Griffith Company

Assistant Project Manager

Brea, CA · On-site

$105K - $125K/yr

We are looking for an Assistant Project Manager to join our Landscape Division. This position is responsible for assisting the Project Manager in providing overall administrative and technical ...

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All JobsClinical Project JobsAssistant Clinical Project Manager JobsAssistant Clinical Project Manager Jobs in Riverside, CA

Assistant Clinical Project Manager information

See Riverside, CA salary details

$33.4K

$76.2K

$121.5K

How much do assistant clinical project manager jobs pay per year?

As of Sep 6, 2026, the average yearly pay for assistant clinical project manager in Riverside, CA is $76,225.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,800.00 and $91,800.00 per year, depending on experience, location, and employer.

What is an assistant clinical project manager?

Assistant Clinical Project Managers are professionals who support the planning, coordination, and execution of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They work under the supervision of Clinical Project Managers to ensure that studies are conducted according to regulatory guidelines, timelines, and budgets. Their responsibilities often include tracking project progress, maintaining documentation, coordinating with cross-functional teams, and addressing issues that arise during clinical studies. This role is vital in ensuring that clinical projects run smoothly and efficiently, ultimately supporting the development of new medical treatments.

How does an assistant clinical project manager typically collaborate with cross-functional teams during a clinical trial?

An Assistant Clinical Project Manager works closely with various teams, including clinical research associates, regulatory affairs, data management, and quality assurance, to ensure successful trial execution. They often coordinate meetings, track project timelines, and facilitate communication between internal stakeholders and external vendors. This collaboration ensures that all regulatory requirements are met and that the study stays on schedule, making strong organizational and interpersonal skills essential for success in the role.

What are the key skills and qualifications needed to thrive as an assistant clinical project manager, and why are they important?

To thrive as an Assistant Clinical Project Manager, you need a solid understanding of clinical research processes, regulatory guidelines (such as GCP), and a relevant degree in life sciences or a related field. Familiarity with project management tools (like MS Project), clinical trial management systems (CTMS), and sometimes certifications such as PMP are valuable assets. Strong organizational, problem-solving, and interpersonal communication skills set candidates apart in this role. These skills and qualifications are critical for ensuring clinical trials run efficiently, compliantly, and collaboratively from start to finish.

What is the difference between Assistant Clinical Project Manager vs Clinical Project Manager?

AspectAssistant Clinical Project ManagerClinical Project Manager
CredentialsBachelor's degree, relevant certifications often preferredBachelor's or higher, certifications like PMP beneficial
Work EnvironmentSupports project teams, assists in coordinationLeads projects, oversees planning and execution
Employer & Industry UsagePharmaceutical, biotech, clinical research organizationsSame industries, higher responsibility
Search & Comparison IntentYesYes

The Assistant Clinical Project Manager typically supports the Clinical Project Manager by handling specific tasks and assisting in project coordination. The Clinical Project Manager holds a leadership role, overseeing the entire project lifecycle, making strategic decisions, and managing teams. Both roles are essential in clinical research, but the Assistant role is more entry-level and supportive, while the Clinical Project Manager has greater responsibility and authority.

What are popular job titles related to Assistant Clinical Project Manager jobs in Riverside, CA?

For Assistant Clinical Project Manager jobs in Riverside, CA, the most frequently searched job titles are:

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

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

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

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

Assistant Clinical Project Manager jobs near you
Infographic showing various Assistant Clinical Project Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 88% Full Time, and 12% Contract. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $76,225 per year, or $36.6 per hour.

Clinical Project Coordinator

Motion Recruitment Partners, LLC

Irvine, CA • On-site

Other

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago

Key responsibilities

  • Track and ensure the completeness of study documents and manage the Trial Master File (v-TMF).

  • Support project teams by tracking study milestones, managing study data, and assisting with study-related communications and documentation.

  • Assist with coordinating study activities such as site payments, ordering and tracking study supplies, and preparing for audits.

Job description

Clinical Project Coordinator
Kelly Science and Clinical FSP is currently seeking a Clinical Project Coordinator for a remote opportunity supporting our Medical Device client. 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 will be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You will also be eligible for paid time off, including holiday, vacation, and sick/personal time.
Summary:
This individual will provide support to the clinical study staff
Perform a variety of clinical research operations duties of a routine and technical nature in support of clinical trials. This includes tracking study documents and management of the Trial Master File (v-TMF).
Supports project managers within the assigned clinical studies.
Key Job Activities:
  • Accountable for tracking essential documents and ensuring completeness of the v-TMF.
  • Assist study staff and Administrative Clinical Study Administrators (aCSA) to quickly resolve issues relating to the v-TMF. Identifies problems and assists in implementing corrective and preventive actions.
  • Manages and supports ongoing use of the Clinical Trial Management System (CTMS) and tracking study milestones and activities.
  • Provide safety documentation to other functional groups in support of safety committee meetings as requested.
  • 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 providing internal communication of important clinical data and events.
  • Assist with tracking site payments.
  • 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.
  • 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, including process improvement activities related to the v-TMF/CTMS.
  • May be involved in other tasks to support the Scientific Affairs Clinical department and Operating Company as needed.

Education:
Minimum of a Bachelor's Degree is required.
Experience
Previous clinical research experience preferred
Requires previous administrative support experience or equivalent for at least 1 year.
Clinical/medical background preferred
Knowledge
Requires experience and knowledge working with computer systems (Microsoft office - Excel, Word and Power Point). Demonstrated competencies in the following areas are required:
Tracking
Written and verbal communications
Attention to details
Organizational skills

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