This Assistant Clinical Research Manager (ACRM) position will work within the clinical research program and assist in the management of the Center of Cancer Therapeutic Innovation (CCTI) research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. These positions, in …
Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate …
The Clinical Research Coordinator will support the Breast Oncology Cohort Studies Program and its clinical and translational 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 for screening and tracking of …
The Clinical Research Coordinator work within the Center of Cancer Therapeutic Innovation (CCTI) 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 …
The Clinical Research Coordinator work within the Genitourinary (GU) 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 …
The Pediatric Cancer Predisposition program is looking for a Clinical Research Coordinator II to join their group to assist in clinical program and research operations. The successful candidate will be interested in genetics as a specialty and possibly genetic counseling. These positions work within the clinical research program …
The Clinical Research Coordinator work within the Lymphoma 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 …
The Clinical Research Coordinator work within the Neuro 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 …
The Pediatric Solid Tumor Program at Dana-Farber Cancer Institute is seeking to hire a motivated Clinical Research Coordinator (CRC) to work within the Clinical Translational Research Program (CTIP) on trials specific to the Solid Tumor Biology and research portfolio. The pediatric Solid Tumor Program is one of the largest in …
The Clinical Research Coordinator work within the Sarcoma 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 …
The Clinical Research Manager works within the DFCI Multiple Myeloma clinical research program and manages the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Trials Office. The Clinical Research Manager, in collaboration with the program’s …
The Regulatory Affairs Specialist (RAS) positions provides advanced expertise and regulatory support to 600+ investigators and research staff members at DFCI, focusing on standards and techniques for performing job functions typical in the development and/or conduct of FDA regulated research from an operational and regulatory compliance perspective. These positions currently …
The Research Project Manager (RPM) I will work within the Cohort Studies Program in the Department of Breast Oncology. This position will be responsible for assigned day-to-day coordination and overall management of activities in cohort studies. Responsibilities include coordinating cohort studies activities and related studies, providing training to research staff, …
The Zakim Center for Integrative Therapies and Healthy Living is recruiting a Research Project Manager I (RPM I). The RPM I is a critical member of the research team who will work on research projects focused on integrative therapies, such as exercise, nutrition, and other supportive care, in oncology patients. …
The Research Project Manager (RPM) is responsible for assigned day-to-day coordination and overall management of sponsor activities for assigned clinical trials; primarily multi-center, PI-initiated trials. Sponsor 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 …
The CTO PI-Initiated Research Project Manager (CTO RPM) for Waldenstrom’s Macoglobulinemia Think Tank Network (WM-NET) is responsible for assigned day-to-day coordination and overall management of WM-NET activities for assigned clinical trials and program; primarily multi-center, PI-initiated trials. Activities include coordinating trial startup and site startup activities, providing training to participating …
The Regulatory Affairs Specialist (RAS) positions provides advanced expertise and regulatory support to 600+ investigators and research staff members at DFCI, focusing on standards and techniques for performing job functions typical in the development and/or conduct of FDA regulated research from an operational and regulatory compliance perspective. These positions currently …
Read more about ""The Clinical Research Coordinator work within the Center of Cancer Therapeutic Innovation (CCTI) 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 …
Read more about ""The Clinical Research Coordinator work within the Sarcoma 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 …
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