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 …
The Project Manager II – Operations & Training manages and executes moderately complex projects that strengthen operational workflows and training programs across the Pediatric Clinical and Translational Investigation Program (CTIP). The role plans and coordinates project activities, resources, timelines, and deliverables; develops and maintains SOPs and process documentation; and builds …
The Protocol Scheduler is responsible for all aspects of patient scheduling for patients on clinical trials, in accordance with department and protocol specific scheduling guidelines. Provides superior customer service to all patients, family members, physicians and staff at all times in accordance with the DFCI Customer Service Standards. Assigned to …
The Protocol Scheduler is responsible for all aspects of patient scheduling for patients on clinical trials, in accordance with department and protocol specific scheduling guidelines. Provides superior customer service to all patients, family members, physicians and staff at all times in accordance with the DFCI Customer Service Standards. Assigned to …
Reporting to the Senior Director of Radiation Oncology Operations, the Quality and Safety Director leads comprehensive quality improvement programs across the Department of Radiation Oncology. This position holds department-wide responsibility for establishing radiation oncology performance standards that align with departmental objectives, institutional requirements, and regulatory mandates through active engagement with …
The Regulatory Compliance Director is a key part of the Compliance team, collaborating across all areas of the organization with a focus on creating a culture of trust and ethical conduct and promoting detection and prevention of conduct that does not align with DFCI’s ethical standards, federal and state healthcare …
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 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, …
The Release Manager supports the implementation and ongoing delivery of our enterprise Workday platform and UKG Pro Workforce Management system within the Business Applications team. This role is key to managing the planning, coordination, and execution of integrated releases across Workday HCM, Payroll, Financials, Supply Chain, Grants Management, and custom …
This is a remote position with occasional time on campus. The selected candidate must live and work from one of the New England states (ME, NH, VT, MA, RI, CT) Reporting to the Director of Finance Systems Transformation, the Research Accounting Systems Strategist provides tactical and strategic systems design …
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 Gastrointestinal (GI) Oncology Clinical Research Program at Dana-Farber Cancer Institute is seeking a Research Data Specialist (RDS) to join our program. 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, stomach, liver, …
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 Research Grants and Publications Coordinator in the Division of Gynecologic Oncology plays a crucial role in managing and facilitating the lifecycle of research grants and publications. This position is responsible for the preparation, submission, and management of federal, non-federal, and foundation grants, ensuring compliance with all relevant regulations and …
The Research Nurse in collaboration with the physician, is responsible for the implementation and evaluation of clinical research in their specific program/area. The CRN has expert knowledge of cancer as a disease process, cancer treatment modalities (or comparable knowledge for a non-oncology area, e.g. infection control) and the process of …
The Research Nurse in collaboration with the physician, is responsible for the implementation and evaluation of clinical research in their specific program/area. The CRN has expert knowledge of cancer as a disease process, cancer treatment modalities (or comparable knowledge for a non-oncology area, e.g. infection control) and the process of …
Within the Department of Cancer Immunology and Virology, the Research Operations Assistant will be required to help keep up with various laboratory and experimental needs for the department. This includes to facilitate and carry out operations activities in the research laboratories. Located in Boston and the surrounding communities, Dana-Farber …
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 ""This is a hybrid position, 4 days oniste, 1 day remote. Monday - Friday 8am - 4:30pm schedule. The selected individual for this position will be required to reside and work within New England (MA, ME, NH, CT, RI, VT). The International Patient Records Specialist is responsible for the …
Read more about ""The Assistant Clinical Lab Supervisor under the guidance of the Supervisor works in a clinical laboratory environment and performs all clinical tests in the designated area(s) of responsibility including providing guidance to staff. The Assistant Supervisor is responsible for compliance with all regulatory requirements as they pertain to the laboratory. …
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