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 Center for Population Sciences at the Dana-Farber Cancer Institute is looking to hire a self-motivated individual for a non-laboratory research assistant position. The research assistant will work with a medical oncology researcher who focuses on health services and outcomes for patients with hematologic malignancies. One specific project is …
The Research Data Specialists (RDS) will support the 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 Data Specialist will be …
The Research Data Specialist (RDS) will support the Hematologic Malignancy Data Repository (HMDR) within the Heme Malignancy clinical research program at Dana-Farber Cancer Institute, under the auspices of the Principal Investigator, Dr. Coleman Lindsley, in the areas of data collection, computing, and database organization ( https://lcdr.dana-farber.org and https://lindsleylab.dana-farber.org ). These …
The Research Data Specialists will support the Thoracic Oncology 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 Research Data Specialist …
The Research Project Manager I is responsible for the day-to-day coordination and management of clinical trial activities, primarily focusing on multi-center, PI-initiated trials. They ensure trial and site startup coordination, train site research staff, handle regulatory submissions, track safety events, and communicate with regulatory authorities. Reporting to faculty, research and/or …
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 …
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 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 …
Read more about ""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 …
Read more about ""The Center for Population Sciences at the Dana-Farber Cancer Institute is looking to hire a self-motivated individual for a non-laboratory research assistant position. The research assistant will work with a medical oncology researcher who focuses on health services and outcomes for patients with hematologic malignancies. One specific project is …
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