The Cell Therapy Clinical Authorization Specialist is responsible for the comprehensive coordination and management of all prior authorization activities specific to cellular therapy services. This includes but is not limited to autologous and allogeneic stem cell transplants, Gene Therapy, chimeric antigen receptor (CAR) T-cell therapy, and other immune effector cell …
The Clinical Research Coordinator 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. The CRC will be responsible for the primary data collection and management of patient clinical information as …
The Clinical Trial Office Clinical Research Coordinator (CRC) 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(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the …
The Research Data Specialists will support the Thoracic clinical research program in the areas of data collection, computing, and database organization. Duties include the examination, synthesis, and evaluation of medical records; the abstraction and recording of pertinent medical information; and the monitoring of patient status. The Clinical Data Specialist will …
The Research Project Manager (RPM) is responsible for assigned day-to-day coordination and overall management of activities for assigned clinical trials. Activities include coordinating trial startup and site startup activities, providing training to participating site research staff, regulatory submissions, safety event tracking and reporting, deviation/violation tracking and reporting, participant accrual tracking …
This position's work location is fully remote with the ocassional time onsite as needed. The Sr. Medicare Coverage Analyst (MCA) is responsible for reviewing clinical research protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant study-related documents to create a coverage analysis/billing guide. The coverage analysis indicates which …
The Clinical Trial Office Clinical Research Coordinator (CRC) 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(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the …
Read more about ""The Clinical Research Coordinator (CRC) will support the Young Women’s program and related breast oncology division and its clinical research in the areas of screening, recruitment, data collection, assurance of high quality data, biospecimen collection and database organization. Duties include the examination, synthesis, and evaluation of medical records and the …
Read more about ""The Professional Development Specialist II (PDSII) is a member of the nursing leadership team. The PDSII is dedicated to advancing the clinical skills and knowledge of nursing staff through comprehensive curriculum design, implementation, and evaluation. This role is crucial in fostering a culture of continuous learning and ensuring adherence to …
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