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Clinical Project Associate Jobs in Massachusetts

Verastem

Clinical Trial Associate

Boston, MA · On-site

$86K - $100K/yr

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 ...

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 projects, working with the study team in the initiation, maintenance and closeout of clinical projects ...

eGenesis

Associate Director, Clinical Science

Cambridge, MA · On-site

$175 - $226/hr

The Associate Director, Clinical Science is responsible for the planning, execution and operational ... Support the design and implementation of early and late-stage clinical projects and ensure that the ...

RSM

Supervisor - Epic Clinical Analyst

Boston, MA

We are currently seeking anEpic Clinical Subject Manager & Project Manager to join our Healthcare ... Supervise associates and senior associates by reviewing work quality, providing coaching, assigning ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA

$75K - $140K/yr

Clinical Trial Associate/ Senior Clinical Trial Associate Skyhawk Therapeutics is seeking a highly ... Demonstrated multi-tasking and project management skills. Skyhawk Therapeutics is committed to pay ...

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All JobsClinical Project Associate JobsClinical Project Associate Jobs in Massachusetts

Clinical Project Associate information

See Massachusetts salary details

$13

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How much do clinical project associate jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical project associate in Massachusetts is $34.45, according to ZipRecruiter salary data. Most workers in this role earn between $23.12 and $45.43 per hour, depending on experience, location, and employer.

What is a clinical project associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a clinical project associate?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a clinical project associate?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

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

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What are the most commonly searched types of Clinical Project jobs in Massachusetts?

The most popular types of Clinical Project jobs in Massachusetts are:

What are popular job titles related to Clinical Project Associate jobs in Massachusetts?

For Clinical Project Associate jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Clinical Project Associate jobs in Massachusetts look for?

The top searched job categories for Clinical Project Associate jobs in Massachusetts are:

What cities in Massachusetts are hiring for Clinical Project Associate jobs?

Cities in Massachusetts with the most Clinical Project Associate job openings:

Clinical Project Associate jobs near you
Infographic showing various Clinical Project Associate job openings in Massachusetts as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 15% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $71,647 per year, or $34.4 per hour.

Clinical Trial Associate

Verastem

Boston, MA • On-site

$86K - $100K/yr

Full-time

Re-posted 22 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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