Clinical Research Coordinator - Breast Oncology
Listed on 2026-03-01
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Healthcare
Clinical Research, Medical Science
Clinical Research Coordinator - Breast Oncology
The Clinical Research Coordinator (CRC) works within the Breast Oncology clinical research program, supporting the research team in the conduct of clinical trials under Good Clinical Practice. Responsibilities include primary data collection, patient sample handling, regulatory binder maintenance, and communication with sponsors and investigators. The CRC may also screen patients for protocol eligibility, obtain informed consent, and collaborate with study departments to ensure study compliance and timely reporting.
Responsibilities- Manage data collection and reporting, including source document capture, adverse event reporting, and resolution of data queries.
- Maintain regulatory binders, ensure compliance with IRB, state, federal, and institutional standards, and assist with IRB protocol submissions and amendments.
- Coordinate sample collection, preparation, and shipment according to protocol and IATA/DOT regulations.
- Collaborate with other departments (Protocol Scheduling, Materials Management, Clinical Research Laboratory, Pharmacy, Research Nursing) to support study logistics.
- Organize internal and external auditing and study monitoring visits.
- Communicate with sponsors, regulatory authorities, and study team throughout the trial life cycle.
- Attend to study participant interactions as directed by protocol.
- Bachelor’s Degree or 1 year of experience in a clinical research setting.
- Excellent organization, communication, and detail‑oriented skills.
- Strong interpersonal skills and ability to work with all levels of staff and external contacts.
- Ability to manage time, prioritize workload, and practice discretion with confidentiality guidelines.
- Computer skills, including Microsoft Office.
Interacts with adult and pediatric patients of all ages and backgrounds, may distribute protocol schedules, quality of life surveys, subject diaries, or conduct follow‑up communication with patients.
EEO StatementDana‑Farber Cancer Institute is an equal opportunity employer. We affirm the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.
Location & PayCambridge, MA. Pay Range: $48,100.00 – $54,400.00.
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