This position reports directly to the Director of Inclusion and Workforce Development. A primary focus of this position is to ensure the successful transition of our adult development programs into a Center for Early Career and Advancement designed to support career advancement of staff and increase access to careers at …
Project Manager will report to the Head of AI Operations and Data Science Services group (DX) in the Informatics & Analytics department at Dana-Farber Cancer Center Institute (DFCI), a teaching affiliate of Harvard Medical School. The Project Manager provides project management support for all projects of the DX group. The …
Dana-Farber’s Network, managed by the Business Initiatives and Alliances department, increases access to Dana-Farber’s oncology expertise by developing clinical and non-clinical partnerships throughout New England and the rest of the country. The Network Project Manager will work closely with the Regional/National Alliances team, the International team, the Employer/Payer team, and …
Within the Department of Business Initiatives and Alliances (BIA), the Project Manager III for Dana-Farber Pathways will support the development and execution of the Dana-Farber Pathways solution. Reporting to the Director of Pathways Operations, the Project Manager III will be responsible for managing the clinical content lifecycle of Dana-Farber Pathways …
The International Project Manager will work under the Director of International Strategic Initiatives and closely with the VP of Business Initiatives and Alliances and the Chief Clinical Development Officer to provide project management support and coordination for initiatives related to international business development. In addition to our Longwood Medical Area-based …
Dana-Farber Cancer Institute (DFCI) and Deerfield Management have entered a multi-year collaboration to create the Center for Protein Degradation (CPD) at DFCI led by Drs. Eric Fischer and Nathanael Gray. The goals of the Center for Protein Degradation are to create a next-generation protein degrader platform and interrogate and advance …
Functioning in a case management model, the Protocol Care Specialist provides specialized patient and resource scheduling and coordination for higher risk clinical services requiring significant knowledge of protocol-defined procedures, regulatory and financial compliance rules. Supporting adult and/or pediatric patients undergoing complex treatment plans and clinical research, the Protocol Care Specialist …
Functioning in a case management model, the Protocol Care Specialist provides specialized patient and resource scheduling and coordination for higher risk clinical services requiring significant knowledge of protocol-defined procedures, regulatory and financial compliance rules. Supporting adult and/or pediatric patients undergoing complex treatment plans and clinical research, the Protocol Care Specialist …
The Purchasing Specialist for Pharmacy provides inventory support to the Pharmacy Department, under the supervision of a licensed pharmacist. The Purchasing Specialist primary responsibility is to ensure we have the right drugs and supplies on-hand when and where we need them. In addition, the purchasing specialist meets with representatives of …
The QA/QI Specialist is responsible for monitoring operations and developing and managing quality improvement initiatives to ensure that systems are safe, effective, appropriate, compliant, current and adhered to by staff in the assigned unit or department. Expected to understand and apply principles of quality management practices to the monitoring and …
Located in Boston and the surrounding communities, Dana-Farber Cancer Institute brings together world renowned clinicians, innovative researchers and dedicated professionals, allies in the common mission of conquering cancer, HIV/AIDS and related diseases. Combining extremely talented people with the best technologies in a genuinely positive environment, we provide compassionate and comprehensive …
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies …
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies …
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies …
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies …
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies …
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies …
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies …
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies …
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s) and/or Clinical Research Manager for Pediatric Neuro-Oncology to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies to ensure regulatory …
