These positions 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 primary data collection and management of …
Under general supervision of the Clinical Research Budgets Manager, the Clinical Research Financial Analyst (CRFA-II) is responsible for financial planning, developing budgets, negotiating financial agreements with funding sources and vendors, and ensuring effective financial management throughout the lifecycle of Clinical Research studies. Handles moderately complex issues and problems and refers …
This position's work location is remote with occasional time onsite as needed. The selected candidate may only work remotely from a New England state (ME, VT, NH, MA, CT, RI). The Office of Data Quality (ODQ) provides research support to the Dana-Farber/Harvard Cancer Center with a focus on quality …
This position's work location is remote with occasional time onsite as needed. The selected candidate may only work remotely from a New England state (ME, VT, NH, MA, CT, RI). The Manager, Clinical Trials Registry is responsible for overseeing the management, compliance, and operational efficiency of Dana-Farber/Havard Cancer Center’s …
The Regulatory Coordinators (RC) work under the direction of the Regulatory Operations Manager to complete the regulatory requirements of the Gastrointestinal Oncology (GI) 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 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 Thoracic Oncology team is hiring a Regulatory Coordinator! The Regulatory Coordinator is the compliance and documentation lead for clinical trials across the thoracic oncology portfolio (e.g., lung cancer, mesothelioma). You will drive study start‑up and ongoing regulatory maintenance to ensure trials are opened quickly and conducted safely, ethically, …
Under minimal supervision, the Senior Clinical Research Accounting Specialist is responsible for billing reconciliation and accounts payable and assists with accounts receivable and reconciliation of financial transactions generated from Dana-Farber Cancer Institute Clinical Research activity. Handles complex issues and problems and refers only the most complex issues to the Clinical …
The Senior Director, Clinical Trials Office (CTO) supports department teams and functions across Dana-Farber Cancer Institute’s (DFCI) Longwood Medical Area campus essential for clinical research operations. Teams and functions include clinically facing clinical research management; regulatory affairs; training and education; and project management and monitoring programs. The Senior Director CTO …
This position's work location is fully remote with the ocassional time onsite as needed. The selected candidate may work remotely from Washington D.C. or any state in the U.S. (except Hawaii). The Sr. Medicare Coverage Analyst (MCA) is responsible for reviewing clinical research protocols, Informed Consent Forms, Clinical Trial …
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 Regulatory Operations 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 …
Read more about ""The Thoracic Oncology team is hiring a Regulatory Coordinator! The Regulatory Coordinator is the compliance and documentation lead for clinical trials across the thoracic oncology portfolio (e.g., lung cancer, mesothelioma). You will drive study start‑up and ongoing regulatory maintenance to ensure trials are opened quickly and conducted safely, ethically, …
Read more about ""Dana-Farber’s Division of Population Sciences is seeking a Clinical Research Coordinator II to support a multidisciplinary, multi-center implementation project designed to improve participation of underrepresented patients in blood cancer research across the Dana-Farber network. Building on extensive institutional efforts to expand access to clinical trials, this role will coordinate complementary …
Read more about ""