The Assistant Clinical Research Manager (ACRM) position will work within the Head & Neck Oncology clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. These positions, in collaboration with …
The Clinical Research Coordinator will support clinical and translational research effort at Breast Oncology Center 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 patients for banking …
The Clinical Research Coordinator work within the Breast 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 Clinical Research Coordinator (CRC) will work within the Center of Cancer Therapeutic Innovation (CCTI) department supporting the clinical research program and 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 …
The Clinical Research Coordinator will work closely with Lachelle D. Weeks MD, PhD, an investigator in the Division of Population Sciences and Director of the CHIP Clinic in the Center for Early Detection and Interception of Blood Cancers. Dr. Weeks’s research focuses on identifying patients at risk for developing the …
The Gastrointestinal (GI) Oncology Clinical Research Program at Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator (CRC) to join the clinical research team. The GI Oncology Clinical Research Program supports PI initiated, industry sponsored, and cooperative group phase I - IV clinical trials across multiple GI cancers, including esophageal, …
The Clinical Research Coordinator work within the Genitourinary Oncology (GU) 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 …
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 …
The Clinical Research Coordinator work within the Dana-Farber Regional Campus 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 disease programs. The Regional Campus CRC will be responsible for the …
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 …
The Clinical Research Project Manager I is responsible for the day-to-day coordination and management of Cutaneous Oncology 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 …
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) works under the direction of the Breast Oncology Principal Investigator(s), Regulatory Operations Manager, 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 …
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 …
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, …
The Research Data Specialist (RDS) will support the Genitourinary Oncology (GU) 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 Clinical …
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 Clinical Data Specialist …
The Project Manager (PM) will play a key role in overseeing the daily coordination and overall research project management of assigned Breast Oncology Cohort Studies and related Secondary Use protocols, working under the guidance of the Principal Investigator(s) (PI) and the Associate Director of Translational Research in the Breast Oncology …
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 …
The Clinical Research Coordinator will support clinical and translational research effort at Breast Oncology Center 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 patients for banking …
Read more about ""The Gastrointestinal (GI) Oncology department is seeking a Translational Research Project Manager I (TRPM I) to support the Translational Research Program. This role will lead colorectal research projects, which may involve collaborations with domestic and international sites to obtain human specimens, collect data, and advance other innovative studies. The …
Read more about ""The Research Data Specialist (RDS) will support the Genitourinary Oncology (GU) 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 Clinical …
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