Upvote
Downvote
Clinical Research Coordinator
Share Job
- Suggest Revision
Full-time
- This position within the Division of Cancer Genetics and Prevention in collaboration with faculty investigators and the research team will support the research team in the overall conduct of national/and or institutional projects related to cancer prevention, early identification of individuals at high risk for cancer, and biorepository collections, using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office.
- The Clinical Research Coordinator (CRC) will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical studies, ensures the timely collection and management of protocol-related samples, maintains regulatory binders, and ensures study compliance with state, federal, and IRB requirements.
- The CRC may be responsible for IRB protocol submissions (including amendments, continuing reviews, and minimal risk protocols), screening patients for protocol eligibility, obtaining informed consent and related participant registration.
- Located in Boston and the surrounding communities, Dana-Farber Cancer Institute brings together world renowned clinicians, innovative researchers and dedicated professionals, allies in the common mission of conquering cancer, HIV/AIDS, and related diseases.
- Oversight of research study start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities
Active Job
Updated TodaySimilar Job
Relevance
Active