This is Part-Time; 24 hours/week role Under direct supervision of the Senior Clinical Research Accounts Specialist, the Clinical Research Accounting Coordinator is responsible for accounts creation and accounts receivable of financial transactions generated from Dana-Farber Cancer Institute Clinical Research activity. Handles basic issues and problems and refers more complex issues …
The CRC (Clinical Research Coordinators) work within the Clinical Research Coordinator - Early Detection & Interception Blood Cancers non-interventional clinical research programs 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 Office of Data Quality (ODQ) provides research support to the Dana-Farber/Harvard Cancer Center with a focus on quality assurance, quality control, and process improvement. Functions of ODQ include protocol subject registration and randomization, clinical research auditing, data and safety monitoring, quality control of DF/HCC initiated clinical trial data, national …
The Symptom Management program at Dana-Farber seeks to re-engineer how Dana-Farber provides care for the side effects of cancer treatment across clinical practice locations. The Project Manager, Symptom Management will lead program strategy and governance and execute deliverables that improve how doctors and nurses work. Reporting to the Senior Director, …
The Senior Clinical Research Manager (CRM) provides strategic and operational oversight of the adult medical oncology clinical trial portfolio across six regional satellite locations within the Greater Boston and Southern New Hampshire areas, including Brighton, Milford, Weymouth, Methuen, Foxborough, MA & Londonderry, NH and any future satellite regional campus. The …
The CRC (Clinical Research Coordinators) work within the Clinical Research Coordinator - Early Detection & Interception Blood Cancers non-interventional clinical research programs 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. …
Read more about ""The Clinical Research Project Manager I is responsible for the day-to-day coordination and management of Breast Oncology clinical trial activities, primarily focusing on multi-center, PI-initiated trials. They ensure trial and site startup coordination, train site research staff, handle regulatory submissions, track safety events, and communicate with regulatory authorities. Reporting to …
Read more about ""The Clinical Research Project Manager (CRPM I) is responsible for the day-to-day coordination and management of Sarcoma clinical trial activities, primarily focusing on multi-center, PI-initiated trials. They ensure trial and site startup coordination, train site research staff, handle regulatory submissions, track safety events, and communicate with regulatory authorities. Reporting to …
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