Clinical Trials Data & Compliance Coordinator
Listed on 2026-10-16
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Healthcare
Clinical Research
Dana-Farber Cancer Institute seeks a Clinical Research Coordinator to support trial conduct under GCP. You will collect and manage patient data, facilitate assessments, and ensure compliance with IRB requirements and study protocols. Collaboration with multiple departments and potential travel are involved.
The role emphasizes meticulous data entry, binder maintenance, and regulatory support to uphold trial integrity and patient safety. A Bachelor’s Degree and CRC experience are preferred.
This role, Clinical Trials Data & Compliance Coordinator at Dana-Farber Cancer Institute, could be your next opportunity.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Clinical Trials Data & Compliance Coordinator role in the description above.
We appreciate your interest in this position.
Join Dana-Farber Cancer Institute and contribute to our ongoing work.
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