Clinical Trials Coordinator II — Data & Compliance Lead

Dana-Farber Cancer Institute

Boston, Northern (MA, KY)

On-site

USD 56,000 - 64,000

Full time

5 days ago

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Job summary

Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator to support the conduct of clinical trials under GCP. You will collect and manage participant data, facilitate trial assessments, and maintain essential regulatory binders to ensure compliance with IRB and protocol requirements.

Responsibilities include screening for protocol eligibility, obtaining informed consent for non-treatment trials, registering participants in ONCORE, and coordinating with departments to support trial

Qualifications

Bachelor's degree required or 2 years of relevant experience.

Responsibilities

Oversee data collection and management of patient clinical information for trials.
Ensure timely trial assessments per protocol and collect protocol-related samples.
Maintain trial binders and regulatory binders to ensure compliance with state, federal, and IRB requirements.
Assist with IRB submissions and protocol eligibility screening as needed.
Register study participants in ONCORE and support trial management activities.
Coordinate with multiple departments to support trial start-up, conduct, and close-out.
Assist with audits and study monitoring visits as needed.
Interact with study participants and ensure adherence to protocols.