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Associate Clinical Project Manager Jobs (NOW HIRING)

Depending on scope and phase of project, may support multiple projects. โ€ข Provides project management expertise throughout the development and implementation of clinical studies. Interacts with ...

Sets quality and compliance goals for the trial and monitors/manages compliance as part of clinical project management. Developsadditionalproject management tools to improve clinical trial ...

Sets quality and compliance goals for the trial and monitors/manages compliance as part of clinical project management. Developsadditionalproject management tools to improve clinical trial ...

... with the Associate Director of Clinical Operations along with the US Site Head. Location ... Provides updates on project status and deliverables to Clinical Project Management leads ...

... 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 ...

... 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 ...

Clinical Project Manager

Durham, NC ยท 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 ...

Clinical Trial Project Management Job Category: Professional All Job Posting Locations: Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville ...

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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 Aug 16, 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?

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.

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Infographic showing various Associate Clinical Project Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $80,597 per year, or $38.7 per hour.

Associate Clinical Project Manager / Clinical Project Manager

n-Lorem

San Diego, CA โ€ข On-site

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago


Job description

Description:

Reporting to: Senior Director, Clinical Operations and Project Management

Hours: Full-Time

Location: Onsite or Hybrid in San Diego, CA

Compensation: $80K-$100K


n-Lorem Foundation

Though n-Lorem is pioneering a novel non-profit model, to provide personalized experimental ASO treatments for free, for life to patients with the rarest of mutations (nano-rare), we are functionally a biotechnology company. We have a large and growing portfolio of ASO medicine discovery programs, ASO medicines in development and multiple clinical programs.

With a seasoned leadership team and strategic partnerships, the n-Lorem Foundation provides the framework, funds and access for nano-rare patients who are amenable to our technology to receive personalized ASO medicines for free, for life. We hope that you will consider joining us as we strive to change the world, one nano-rare patient at a time.

If you are a clinical project manager who champions organization, excellent communication (both written and verbal), efficiency and attention to detail. This role is well suited for someone who is motivated by purpose and impact, and who wants to contribute to a team united by the belief that we can change the world—one patient and one family at a time.


Job Overview

n-Lorem is seeking a passionate, organized, detail- and action-oriented individual to join our team as an Associate Project Manager or Project Manager. In this role, you will partner closely with the Senior Director of Clinical Operations and Project Management and the Vice President of Clinical Development. The successful candidate will help to manage n-Lorem’s portfolio of patients by working closely with a cross-functional team. You will be committed to excellent documentation, timeline management, process improvement, and efficiency. You will also ensure activities are streamlined within the organization based on rapidly evolving development and operational priorities. Your day-to-day activities will focus on the advancement of all n-Lorem Patient ASO programs and business operations activities to meet the needs of our patients and internal team. In general, you will assist the clinical operations and program management leadership teams with tasks such as ensuring consistent documentation across the n-Lorem portfolio, detailed record keeping of project details and communications, and working with a multi-disciplinary team to facilitate communication and forward progress of all patient programs. No two days will be the same and flexibility will be key as an important member of our fast-paced growing team.


Key Responsibilities:

  • Support the maintenance of centralized locations for all Clinical and Development Operations including dashboards, metrics reports, tools, and databases.
  • Work closely with Clinical Development and Program Management teams to track progress, manage timelines, document key decisions, maintain systems for organizing complex information, and respond to queries.
  • Proactively identify and address potential gaps across the organization to ensure patient programs run smoothly and stakeholders have access to business-critical information to enable decision making.
  • Meeting Planning, Management, and Follow-up, including:
- Scheduling.

- Facilitate group discussions with diverse perspectives across geographies, and bring teams to agreement.

- Development of tailored agendas to each unique patient program.

- Generate meeting minutes and track action items of varying scope and importance to ensure all items owned by you

(and others) are completed in a timely fashion.

  • Manage process to obtain and coordinate receipt of required data and materials for all patient programs.
  • Assist scientific teams with timeline tracking, and conduct periodic analyses of aggregate timeline data.
  • General document management including detailed record keeping and co-authoring process documents and standardized templates.
  • Creation and maintenance of critical external communication lists and team rosters.
  • Proactively identify inefficiencies and propose possible solutions and escalate potential issues.
  • Prepare reports and correspondence to investigators, partners, collaborators, and the n-Lorem leadership team.
  • Act as a liaison between internal n-Lorem teams and physician and institution teams.
  • Prioritize work in a fast-paced environment with evolving project priorities to meet deliverables and objectives.
  • Other duties as assigned to support our quickly-growing multi-disciplinary team.
Requirements:

Requirements:

  • U.S. work authorization.
  • Minimum of a Bachelor’s degree in a scientific or technical discipline.
  • 1-2+ years of experience in Project Management in the pharmaceutical or biotechnology industries.
  • Familiarity with the principles of clinical trial conduct including clinical drug development, clinical trials operations, and regulatory components.
  • Strong and crisp written and verbal communication with excellent customer service skills.
  • Ability to work effectively in a fast-paced, cross-functional environment with multiple stakeholders.
  • A team player who has a strong sense of ownership, accountability, and responsibility.
  • Strong attention to detail, organizational skills, and ability to manage multiple priorities.
  • Experience with Microsoft Office 365 and SharePoint.

n-Lorem offers a competitive benefits package including medical, dental, vision, 403(b), four weeks paid vacation, paid sick time, life insurance, employee assistance program. n-Lorem is a small foundation with an extraordinary mission, to provide hope and potentially help to nano-rare patients. Every employee in our organization is a significant contributor to this mission. We know that our work could have a profound impact on the life of a patient today.

n-Lorem is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. n-Lorem is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know.


For more information on n-Lorem, please visit our website www.nlorem.org