Clinical Trial Associate

Oncology Clinical Trial Associate (Contract, 0.5 FTE)

Location: Boston, Massachusetts (Hybrid)

My client is currently looking for a Clinical Trial Associate with oncology experience for a part‑time, contract position. The role supports clinical trial operations in oncology studies, focusing on regulatory compliance and trial documentation.

Possibility of converting to a permanent position.

Responsibilities:

• Support clinical trial operations for oncology studies.
• Maintain the Trial Master File (TMF), ensuring it is up‑to‑date and inspection‑ready.
• Coordinate and track trial documents, regulatory submissions, and approvals.
• Facilitate communication with internal and external stakeholders.
• Support study start‑up, maintenance, and close‑out activities.
• Assist with tracking and reconciling study data and subject information.
• Help monitor trial timelines and milestones.

Qualifications:

• Bachelor’s degree in life sciences or related field preferred.
• At least 2 years of experience as a Clinical Trial Associate, preferably in oncology.
• Familiarity with GCP, ICH guidelines, and FDA regulations.
• Strong organizational and interpersonal skills.
• Experience with eTMF and CTMS systems preferred.
• Ability to work in Boston, Massachusetts, in a hybrid capacity.

If you are interested,
apply now! - Manager will interview this week and next week for the right candidate.

Seniority level: Associate

Employment type: Contract

Job function: Science, Research, and Administrative

Industries: Research Services, Biotechnology Research, Pharmaceutical Manufacturing