The Clinical Research Coordinator work within the Gynecologic Oncology 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. The CRC will be responsible for the primary data collection and management of patient clinical …
Read more about ""T he 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 …
Read more about ""This Clinical Research Coordinator will be responsible for helping to coordinate a very large Dana-Farber Cancer Institute sample and data collection study. This study is designed to facilitate the identification, storage, and use of specimens during the course of clinical care and includes a component with return of genomic or …
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