Barrington James
Clinical Trial Associate (Contract, 0.5 FTE)
Location:
Boston, Massachusetts (Hybrid)
Position Overview:
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.
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 Administrative, Research, and Science
Industries Research Services, Biotechnology Research, and Pharmaceutical Manufacturing
#J-18808-Ljbffr
Boston, Massachusetts (Hybrid)
Position Overview:
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.
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 Administrative, Research, and Science
Industries Research Services, Biotechnology Research, and Pharmaceutical Manufacturing
#J-18808-Ljbffr