The CRC (Clinical Research Coordinators) work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The CRC will be responsible for the primary data collection and …
Read more about ""The Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies and guidelines, including federal, state, local, as well as the policies and procedures outlined by the Dana-Farber Cancer Institute and Dana-Farber Harvard Cancer Center (DF/HCC) consortium. Under the direction of Clinical Trials …
Read more about ""The Clinical Research Coordinator work within the Multi-Cancer Early Detection Program and the Division of Population Sciences at the Dana-Farber Cancer Institute. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical studies, with a primary emphasis …
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