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Associate Clinical Project Manager Jobs in Boston, MA

Verastem

Clinical Trial Associate

Boston, MA · On-site

$86K - $100K/yr

Coordinates cross function project team meetings with Clinical Project Manager and assists in preparation of agendas, minutes and tracking of action items. * Assists in the creation of study ...

Ora

Clinical Research Coordinator I

Andover, MA · On-site

$24.50 - $32.75/hr

Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers ... Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications is strongly ...

Ora

Clinical Research Coordinator I

Andover, MA · On-site

$24.50 - $32.75/hr

Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers ... Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications is strongly ...

Ora

Clinical Research Coordinator I

Andover, MA · On-site

$24.50 - $32.75/hr

Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers ... Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications is strongly ...

Alira Health

Project Manager

Boston, MA · On-site

$115K - $145K/yr

Summary ROLE The Project Manager (PM) is an important member of the Alira Health Clinical team. The ... Supervises and trains Associate PMs. * Creates and reviews clinical study documents, including ...

CAPTIVATE LLC

Associate Project Manager

Lowell, MA

$75K/yr

Associate Project Manager This position will support the Implementation Team (Project Management) with the enablement process for existing and new projects by assisting the Project Management team ...

New

Creative Cove Inc.

Associate Project Manager

Boston, MA · On-site

Our Downtown Boston AEC client is looking for an onsite Associate Project Manager to support senior members of the team; tasks will range from taking minutes during meetings to overall administrative ...

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... Support the CTM or project manager with study start up and execution * Act as a second point of ...

DTCC

Project Manager Associate

Boston, MA · On-site

As a member of the Enterprise Transformation team, the Project Manager - Associate supports the delivery of business and technology initiatives by partnering closely with senior project and program ...

Apps Associates

Project Manager - IMS

Acton, MA · On-site

Collaborate with Apps Associates project team members, who are both onshore and offshore, to successfully deliver projects * Manage the execution of the project's activities and resources in ...

Apps Associates

Project Manager - IMS

Acton, MA · On-site +1

Collaborate with Apps Associates project team members, who are both onshore and offshore, to successfully deliver projects * Manage the execution of the project's activities and resources in ...

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All JobsAssociate Clinical Project JobsAssociate Clinical Project Manager JobsAssociate Clinical Project Manager Jobs in Boston, MA

Associate Clinical Project Manager information

See Boston, MA salary details

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

As of Aug 11, 2026, the average hourly pay for associate clinical project manager in Boston, MA is $42.15, according to ZipRecruiter salary data. Most workers in this role earn between $32.40 and $48.89 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.

What are the most commonly searched types of Clinical Project Manager jobs in Boston, MA? The most popular types of Clinical Project Manager jobs in Boston, MA are:
What are popular job titles related to Associate Clinical Project Manager jobs in Boston, MA? For Associate Clinical Project Manager jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Associate Clinical Project Manager jobs in Boston, MA look for? The top searched job categories for Associate Clinical Project Manager jobs in Boston, MA are:
What cities near Boston, MA are hiring for Associate Clinical Project Manager jobs? Cities near Boston, MA with the most Associate Clinical Project Manager job openings:
Associate Clinical Project Manager jobs near you
Infographic showing various Associate Clinical Project Manager job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $87,667 per year, or $42.1 per hour.

Clinical Trial Associate

Verastem

Boston, MA • On-site

$86K - $100K/yr

Full-time

Re-posted 18 days ago

Job description

Company Profile:
At Verastem Oncology, we address urgent needs of patients living with cancers driven by RAS/MAPK pathway mutations, a key driver of tumor growth and treatment resistance. FDA approval of AVMAPKI FAKZYNJA CO-PACK delivered the first therapy for women living with recurrent KRAS-mutated low-grade serous ovarian cancer, a rare cancer with significant unmet need. We've launched this novel/novel combination therapy in the U.S. and are exploring pathways for Europe and Japan. We continue to advance our pipeline of drugs to help block cancer cell survival, inhibit tumor growth, and overcome treatment resistance. This is an exciting opportunity to shape the future of cancer care and make a meaningful impact in the lives of patients.
Summary:
Responsible for assisting and providing support to the members of the clinical operations project team to facilitate the operational execution of the clinical trial processes in accordance with regulatory guidelines and ICH/GCP standards.
Responsibilities:
  • Manages trial related documents in the Veeva Vault Trial Master File (TMF); manages user access and facilitate training for internal/external users as needed; trains new users.
  • Uploads and reviews TMF documents for completeness, accuracy and compliance with protocol and applicable regulations, standard operating procedures and best practices.
  • Performs quality checks and follow-up on resolution of open issues to ensure cross functional study team members are compliant with use of required documents within the TMF.
  • Audits TMFs and resolves discrepancies with minimal supervision.
  • Creates and maintains internal folders on company share drive(s).
  • Manages study investigator CDAs, contract approval and purchase order creation.
  • Coordinates cross function project team meetings with Clinical Project Manager and assists in preparation of agendas, minutes and tracking of action items.
  • Assists in the creation of study materials, including but not limited to documents, presentations and reports.
  • Supports CPM to established and maintain the tracking tools for project metrics such as site activation, patient enrollment and site contacts.
  • Reviews and assists in the collection of essential documents for completeness and compliance with SOPs, the protocol and appropriate regulations.
  • Creates and reviews IMP release packet prior to initiation; review background information of potential new sites (e.g. debarment check, Inspection history, etc).
  • Assists study team and sites with preparation for audits/inspections.
  • Participates in inter-departmental workgroups to create or enhance processes.
  • May participate in the training of CRO teams, investigators and study team members.
  • May serve as the point of contact for vendors and oversee selected vendor activities.
  • May be responsible for updating Clintrials.gov.
  • Performs administrative tasks to support team members with clinical trial execution, as needed.

Qualifications:
  • Bachelor's degree or nursing degree is required. Scientific/health care field preferred, but not required.
  • Minimum of 4 years' experience in relevant field (e.g. clinical site, CRO, Sponsor or clinical trial vendor).
  • Relevant experience in clinical research or related field.
  • Adequate Good Clinical Practice training.
  • General knowledge of guidelines governing clinical research.
  • Comfortable with technology and ability to learn new systems quickly.
  • Experienced with Veeva TMF.
  • Strong knowledge of MS Word, Excel, PowerPoint and Outlook.
  • Requires strong attention to detail in composing and proofing materials, establishing priorities, scheduling and meeting deadlines.
  • Must be able to professionally interact and communicate with visitors, vendors and individuals at all levels of the organization.
  • Must be able to work in a fast-paced environment with demonstrated ability to work on multiple competing tasks and demands.
  • Ability to work successfully within a cross-functional team.

The base salary range (86K-100K) provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including job-related skills, experience, internal equity, relevant education or training, location, and market dynamics. In addition, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package.

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