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Associate Clinical Project Manager Jobs (NOW HIRING)

Clinical Project Manager

$119K - $149K/yr

Provide functional guidance and support to Associate Clinical Project Managers as needed. * Other duties as assigned. Education and Experience: Required: * Bachelor's in related discipline required ...

... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...

... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...

... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...

Position Summary: The Clinical Project Manager - OhioRISE Program is a management position ... Requires an associate degree in nursing, LSW/LPC, LISW/LPCC, bachelor's or master's degree in ...

Clinical Project Manager

Durham, NC · On-site

$85K - $120K/yr

As a Clinical Project Manager, you will play a critical role in leading cross-functional teams, ensuring adherence to project timelines, budgets, and quality standards, while collaboratively working ...

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Associate Clinical Project Manager information

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How much do associate clinical project manager jobs pay per hour?

As of Jul 7, 2026, the average hourly pay for associate clinical project manager in the United States is $38.75, according to ZipRecruiter salary data. Most workers in this role earn between $29.81 and $44.95 per hour, depending on experience, location, and employer.

What is an Associate Clinical Project Manager?

An Associate Clinical Project Manager (ACPM) is an entry- to mid-level professional who assists in planning, coordinating, and overseeing clinical trials and research projects within pharmaceutical, biotech, or clinical research organizations. They work closely with project managers and cross-functional teams to ensure studies are conducted according to protocol, regulatory requirements, and timelines. ACPMs may handle tasks such as tracking project progress, supporting site management, preparing documentation, and communicating with stakeholders. Their role helps ensure the smooth execution and delivery of clinical research projects.

What are the common challenges faced by an Associate Clinical Project Manager and how can they be addressed?

Associate Clinical Project Managers often encounter challenges such as balancing multiple study timelines, coordinating cross-functional teams, and ensuring regulatory compliance. Managing communication between sponsors, vendors, and internal teams can also be complex. To address these challenges, it's important to prioritize tasks, maintain clear documentation, and foster strong relationships with stakeholders. Leveraging project management tools and regularly reviewing project milestones can help ensure studies stay on track and issues are promptly resolved.

What are the key skills and qualifications needed to thrive as an Associate Clinical Project Manager, and why are they important?

To thrive as an Associate Clinical Project Manager, you need a solid understanding of clinical research processes, project management principles, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Exceptional organizational skills, attention to detail, and strong communication abilities help you coordinate teams and timelines effectively. These competencies are crucial for ensuring clinical trials run smoothly, meet regulatory standards, and deliver reliable results on schedule.

What is the difference between Associate Clinical Project Manager vs Clinical Project Coordinator?

AspectAssociate Clinical Project ManagerClinical Project Coordinator
CredentialsBachelor's degree, often some project management or clinical research experienceBachelor's degree, entry-level in clinical research
Work EnvironmentSupports project managers, involved in planning and oversightAssists with daily tasks, data collection, and site communication
Employer & Industry UsagePharmaceutical, biotech, clinical research organizationsClinical research sites, CROs, pharma companies

The Associate Clinical Project Manager typically has more responsibility in project planning and oversight compared to the Clinical Project Coordinator, who mainly supports data collection and site coordination. Both roles are essential in clinical research teams, with the associate role often serving as a stepping stone to more senior project management positions.

More about Associate Clinical Project Manager jobs
What cities are hiring for Associate Clinical Project Manager jobs? Cities with the most Associate Clinical Project Manager job openings:
What are the most commonly searched types of Clinical Project Manager jobs? The most popular types of Clinical Project Manager jobs are:
What states have the most Associate Clinical Project Manager jobs? States with the most job openings for Associate Clinical Project Manager jobs include:
What job categories do people searching Associate Clinical Project Manager jobs look for? The top searched job categories for Associate Clinical Project Manager jobs are:
Infographic showing various Associate Clinical Project Manager job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $80,597 per year, or $38.7 per hour.
Associate Clinical Project Manager

Associate Clinical Project Manager

Actalent

Valencia, CA

Full-time

Medical, Retirement

Posted 13 days ago

Be an early applicant


Job description

Job Title: Associate Clinical Project Manager

Must be able to go onsite 1-2x a month in Valencia CA

Growing Medical Device Company!

exposure to both upstream and downstream product process needed!

Job Description

This role focuses on both upstream product management and downstream marketing for products in a regulated environment, with an emphasis on medical devices. You will become a subject matter expert on assigned products, support the full product lifecycle, and partner closely with cross-functional teams to define requirements, shape the product roadmap, and drive effective marketing and communication strategies. This position offers significant exposure to both product and marketing functions and provides a strong foundation for long-term career growth in product management, marketing, or commercial strategy.

Responsibilities

  • Develop clear and detailed product requirements that align with customer needs, regulatory constraints, and business objectives.
  • Serve as the voice of the customer (VoC) by gathering, synthesizing, and translating customer feedback into actionable product insights.
  • Contribute to product roadmap planning, including prioritizing features, enhancements, and lifecycle activities.
  • Create, review, and maintain product labeling in accordance with regulatory and internal standards.
  • Manage ongoing product upkeep and maintenance, ensuring products remain current, compliant, and competitive.
  • Support downstream marketing activities by developing brochures and marketing materials that effectively communicate product value.
  • Plan and support social media campaigns that increase product awareness and engagement.
  • Coordinate e-blasts and digital marketing initiatives to support product launches, promotions, and key campaigns.
  • Develop and refine product positioning and messaging to highlight key value propositions and communicate features clearly and effectively.
  • Act as a true product expert, providing subject matter expertise to internal teams, sales, and external stakeholders.
  • Collaborate closely with cross-functional partners, including project management and product management teams, to ensure alignment across upstream and downstream activities.
  • Support national sales meetings, industry conferences, and trade shows by providing product expertise, marketing support, and on-site representation.
  • Contribute to the planning and execution of activities across different product lifecycle stages, from introduction to maturity and maintenance.
  • Demonstrate a proactive, self-starter approach by identifying opportunities for product and marketing improvements and driving initiatives to completion.

Essential Skills

  • 2–3 years of experience in product management.
  • Experience working in a regulated environment; medical device experience is preferred, with openness to equivalent regulated industries.
  • Demonstrated ability to develop and manage product requirements.
  • Experience contributing to upstream marketing activities such as product roadmap planning and voice of customer initiatives.
  • Experience supporting downstream marketing activities, including marketing collateral, social media, and digital campaigns.
  • Familiarity with product labeling requirements within a regulated context.
  • Strong self-starter and go-getter mentality with the ability to work independently and drive projects forward.
  • Ability to become a subject matter expert on products and communicate technical or clinical information clearly.
  • Strong collaboration skills with the ability to work closely with cross-functional teams.

Additional Skills & Qualifications

  • Experience working in a smaller company or startup environment.
  • Exposure to both upstream and downstream product processes.
  • Familiarity with products at various stages of the lifecycle, including launch, growth, and maintenance.
  • Experience participating in or supporting national sales meetings, industry conferences, and trade shows.
  • Interest in building a long-term career in product management, marketing, or commercial strategy.

Work Environment

This role offers flexibility with openness to remote candidates, with a preference for individuals who can travel to the Valencia office approximately one to two times per month. The primary work will be performed remotely, with occasional onsite presence to collaborate with colleagues and participate in key meetings. Travel is required approximately 25% of the time, with a higher travel load at the beginning of the role. Travel includes attendance at national sales meetings, industry conferences, and trade shows, typically three to four per year, often concentrated in the first quarter. The environment centers on products in a regulated industry, particularly medical devices, and involves regular collaboration with cross-functional teams across product management, marketing, and commercial functions.

Job Type & Location

This is a Permanent position based out of Valencia, CA.

Pay and Benefits

The pay range for this position is $95000.00 - $105000.00/yr.

401k, health benefits, bonus options

Workplace Type

This is a hybrid position in Valencia,CA.

Application Deadline

This position is anticipated to close on Jun 30, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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