Clinical Research Managers work within the clinical research program and manage 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 physicians and research nursing …
These positions work within the clinical research program and manage 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 physicians and research nursing staff, …
The 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 Trials …
The 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 Trials …
The Department of Data Science and the Translational Immunogenomics Lab (TIGL) within the Dana-Farber Center for Immuno-oncology are seeking a highly motivated and skilled computational individual who will work within an interdisciplinary team comprising computational scientists, data scientists, bioinformaticians, physicians, and biomedical scientists on developing analytical pipelines for personalized neoantigen …
The NGS Bioinformatics Group at Dana-Farber Cancer Institute seeks a Computational Biologist to work on Profile, our institutional comprehensive precision cancer medicine initiative. The candidate will work on developing NGS bioinformatic workflows and modules for the analysis of rich and complex somatic and germline data from the Profile project 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 Physician Assistant (PA) is responsible for working with the Attending Physicians in the medical and/or surgical management of renated and unrelated HSCT/CT donors for hematologic and solid tumor oncology standard of care and clinical trial patients. The PA has expert knowledge of medical and/or surgical oncology, incorporating knowledge of …
The Regulatory Affairs Specialist (RAS) is responsible for providing strategic, tactical and operational direction and support to investigators and study teams for working within regulations to expedite the development and delivery of safe and effective healthcare products to DFCI patients and the world. The RAS will work closely and collaboratively …
The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager and / 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 …
The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager and / 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 …
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 Coordinators (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager and / 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 …
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s) and Clinical Research Manager 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 compliance with DFCI …
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 …
The Research Data Specialists will support the clinical research program, under the auspices of the Principal Investigator(s) and the Clinical Trials Office, in the areas of data collection, computing, and database organization. Duties may include but are not limited to; the examination, synthesis, and evaluation of medical records; the abstraction …
The Research Data Specialists will support the clinical research program, under the auspices of the Principal Investigator(s) and the Clinical Trials Office, in the areas of data collection, computing, and database organization. Duties may include but are not limited to; the examination, synthesis, and evaluation of medical records; the abstraction …
The Research Data Specialist (RDS) will support the Gastrointestinal (GI) Oncology Translational Research Program in the areas of patient consenting, sample processing, and data collection. The GI Oncology Translational Research Program supports various aspects of research for GI Cancers. This program is a bridge between clinical care and wet lab …
The Research Data Specialists will support the clinical research program, under the auspices of the Principal Investigator(s) and the Clinical Trials Office, in the areas of data collection, computing, and database organization. Duties may include but are not limited to; the examination, synthesis, and evaluation of medical records; the abstraction …
The Senior Clinical Research Manager will be a key member of the newly established Center for Early Detection & Intervention. The Center aims to redefine the cancer experience by precision prevention, early detection, and interception. The Senior Clinical Research Manager will manage the clinical research team in the overall conduct …
