The Dana-Farber Cancer Institute Division of Population Sciences is currently seeking a Clinical Research Coordinator I to work on cancer research projects that focus on adult patient populations. The Clinical Research Coordinator’s efforts will primarily be focused on enrolling and tracking study participants, administering survey to study participants, medical record …
The Clinical Research Coordinator work within the Bone Marrow Transplant 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 …
A position is immediately available for a Neuropathology Clinical Research Coordinator to join the Precision Medicine Program within the DFCI Department of Pathology. The applicant would be a member of Dr. Keith Ligon’s Lab and the Center for Neuro-oncology at Dana Farber Cancer Center. The candidate will be required to …
The Clinical Research Coordinator will support the Breast Oncology Cohort Studies Program and its clinical and translational research 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 …
The Clinical Research Coordinator work within the Center of Cancer Therapeutic Innovation 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 …
The Center for Early Detection and Interception of Blood Cancers seeks a Clinical Research Coordinator to assist in the day-to-day management of non-interventional trials. This position works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the …
The Clinical Research Coordinator work within the Cutaneous 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 …
The Clinical Research Coordinator work within the Genitourinary 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 Gastrointestinal (GI) Oncology Clinical Research Program at Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator (CRC) 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 Clinical Research Coordinator work within the Gynecologic 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 …
Building upon Dana-Farber’s deep experience in early cancer detection and treatment, we’ve created a robust, integrated clinical/research program -- Centers for Early Detection and Interception. This program brings together Dana-Farber’s expert clinicians and researchers across all cancer types, working together in a unified, multi-disciplinary effort that will accelerate progress in early …
The Clinical Research Coordinator works within the Stem Cell Transplant Immune Effector Cell clinical research program and supports 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 …
The Clinical Research Coordinator work within the Lymphoma 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 …
The Clinical Research Coordinator work within the Melanoma 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 …
The Clinical Research Coordinator work within the Multiple Myeloma 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 …
This Clinical Research & Lab Specialist position 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 Research Manager will work within the Cutaneous Oncology 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 …
The Clinical Research Manager (CRM) will work within the Genitourinary Oncology (GU) 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 Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Regulatory Operations Manager, and Clinical Research Manager to complete the regulatory requirements of the Leukemia clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies to ensure …
Dana-Farber is seeking a highly motivated individual to provide support for several research studies within the Department of Supportive Oncology. Broadly, research projects focus on the development and testing of novel behavioral treatments (e.g., mobile health apps, tele-health delivery) for patients with cancer and chronic pain or who are at …
The Clinical Research Coordinator work within the Gynecologic 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 …
Read more about ""T he 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 …
Read more about ""This Clinical Research Coordinator will be responsible for helping to coordinate a very large Dana-Farber Cancer Institute sample and data collection study. This study is designed to facilitate the identification, storage, and use of specimens during the course of clinical care and includes a component with return of genomic or …
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