Confidential
Clinical Trial Associate (Oncology) – Hybrid (Boston)
Boston, MA | Hybrid (3 days onsite)
About the Opportunity A growing clinical‑stage oncology company advancing multiple early‑phase programs is seeking an experienced
Clinical Trial Associate (CTA)
to support ongoing clinical operations activities. You will play a key role in ensuring high‑quality trial execution and maintaining inspection‑ready TMFs across both internal and CRO‑managed systems.
What You’ll Do
Support
3–4 active oncology studies
in collaboration with Clinical Trial Managers and cross‑functional teams
Maintain, update, and QC
TMF filing
across internal and CRO‑managed TMFs
Manage clinical trackers (MVR logs, enrollment trackers, decision logs, etc.)
Generate and QC
meeting minutes , including vendor and cross‑functional meetings
Assist with preparation of study documents, presentations, and operational materials
Coordinate study team meetings and support day‑to‑day clinical operations
Ensure documentation quality and proactively identify gaps or issues
What You Bring Technical Experience
Strong background supporting
oncology clinical trials
Hands‑on experience with
TMF systems
and TMF specifications
Familiarity with
ClinTrak, Trial Interactive, and/or Veeva
Ability to maintain clinical trackers and support operational documentation
Soft Skills
Excellent communication, organization, and documentation abilities
Ability to manage multiple studies and shifting priorities
Proactive, detail‑oriented, and solutions‑focused mindset
Strong collaboration skills with the ability to work independently or closely with CTMs
Seniority level Mid‑Senior level
Employment type Contract
Job function Research
Industries Pharmaceutical Manufacturing and Public Health
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Boston, MA | Hybrid (3 days onsite)
About the Opportunity A growing clinical‑stage oncology company advancing multiple early‑phase programs is seeking an experienced
Clinical Trial Associate (CTA)
to support ongoing clinical operations activities. You will play a key role in ensuring high‑quality trial execution and maintaining inspection‑ready TMFs across both internal and CRO‑managed systems.
What You’ll Do
Support
3–4 active oncology studies
in collaboration with Clinical Trial Managers and cross‑functional teams
Maintain, update, and QC
TMF filing
across internal and CRO‑managed TMFs
Manage clinical trackers (MVR logs, enrollment trackers, decision logs, etc.)
Generate and QC
meeting minutes , including vendor and cross‑functional meetings
Assist with preparation of study documents, presentations, and operational materials
Coordinate study team meetings and support day‑to‑day clinical operations
Ensure documentation quality and proactively identify gaps or issues
What You Bring Technical Experience
Strong background supporting
oncology clinical trials
Hands‑on experience with
TMF systems
and TMF specifications
Familiarity with
ClinTrak, Trial Interactive, and/or Veeva
Ability to maintain clinical trackers and support operational documentation
Soft Skills
Excellent communication, organization, and documentation abilities
Ability to manage multiple studies and shifting priorities
Proactive, detail‑oriented, and solutions‑focused mindset
Strong collaboration skills with the ability to work independently or closely with CTMs
Seniority level Mid‑Senior level
Employment type Contract
Job function Research
Industries Pharmaceutical Manufacturing and Public Health
#J-18808-Ljbffr