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Tmf Associate Jobs in Boston, MA (NOW HIRING)

Verastem

Clinical Trial Associate

Boston, MA · On-site

$86K - $100K/yr

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 ...

Olema Oncology

Senior Clinical Trial Associate

Boston, MA · On-site

$110K - $115K/yr

About the Role >>> Senior Clinical Trial Associate As the Senior Clinical Trial Associate reporting ... Contributes to the development of the TMF plan and conducts periodic quality control reviews and ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$75K - $140K/yr

Clinical Trial Associate/ Senior Clinical Trial Associate Skyhawk Therapeutics is seeking a highly ... Veeva TMF working knowledge and for senior level, demonstrated knowledge of ICH-GCP, FDA and ...

Relay Therapeutics

Clinical Project Associate

Cambridge, MA · On-site

$61K - $87K/yr

As Clinical Project Associate, you will be accountable for providing clinical trial coordination ... You will help to ensure the Trial Master File (TMF) is up-to-date and inspection ready. * You will ...

Alira Health

Project Manager

Boston, MA · On-site

$115K - $145K/yr

Supervises and trains Associate PMs. * Creates and reviews clinical study documents, including ... Assists in TMF management and manages TMF reviews as needed. * Prepares for and participates in ...

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Showing results 21-40

All JobsTmf Associate JobsTmf Associate Jobs in Boston, MA

Tmf Associate information

See Boston, MA salary details

$18

$43

$76

How much do tmf associate jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for tmf associate in Boston, MA is $43.49, according to ZipRecruiter salary data. Most workers in this role earn between $35.05 and $47.84 per hour, depending on experience, location, and employer.

What is the difference between Tmf Associate vs Tmf Analyst?

AspectTmf AssociateTmf Analyst
Required CredentialsBachelor's degree in life sciences, pharmacy, or related fields; basic knowledge of clinical trial processesBachelor's or master's degree; deeper understanding of TMF processes and regulatory requirements
Work EnvironmentClinical research organizations, pharmaceutical companies, or CROs; supporting TMF documentationMore analytical role within similar settings; involved in reviewing and ensuring compliance
Employer & Industry UsageCommonly used in clinical trial documentation teamsUsed in quality assurance and compliance teams within the same industry

The main difference between a Tmf Associate and a Tmf Analyst lies in their experience level and scope of responsibilities. Tmf Associates typically handle documentation support and basic compliance tasks, while Tmf Analysts perform more detailed reviews and analysis to ensure regulatory adherence. Both roles are essential in clinical trial management, with the Analyst position requiring a deeper understanding of TMF processes.

What are the most commonly searched types of Tmf jobs in Boston, MA? The most popular types of Tmf jobs in Boston, MA are:
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What cities near Boston, MA are hiring for Tmf Associate jobs? Cities near Boston, MA with the most Tmf Associate job openings:
Tmf Associate jobs near you
Infographic showing various Tmf Associate job openings in Boston, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $90,466 per year, or $43.5 per hour.

Clinical Trial Associate

Verastem

Boston, MA • On-site

$86K - $100K/yr

Full-time

Re-posted 17 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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