Working in a fast-paced, high volume, dynamic environment, the Clinical Authorization Specialist will bring clinical expertise to the prior authorization and appeals processes and serve as a liaison and patient advocate between Dana Farber Cancer Institute and various health plans.Reporting to the Prior Authorization Supervisor , the Clinical Authorization Specialist …
The Chemistry Lab Supervisor is responsible for the technical and administrative management of the chemistry laboratory, including general chemistry assays and immunoassays. This position is under the direction of the Administrative Director and the Chemistry Medical Director. The position provides technical supervision on site, and is responsible for the proper …
The Clinical Pharmacist Specialist II - Genitourinary Oncology is responsible for providing clinical pharmacy services to patients in The genitourinary oncology disease center and will work closely with physicians, advanced practice providers, nurses, and pharmacists to provide comprehensive patient care for outpatients. The Clinical Pharmacist Specialist II - Genitourinary Oncology …
The Clinical Pharmacy Specialist for Infectious Disease and Antimicrobial Stewardship is responsible for providing clinical pharmacy services to patients in all ambulatory clinical areas and will partner together with the BWH Department of Infectious Diseases and Antimicrobial Stewardship Services to implement institutional guidelines and engage in process improvement work to …
The Clinical Pharmacy Specialist is responsible for providing clinical pharmacy services to patients in a clinical disease area and will work closely with physicians, mid-level providers, nurses, and pharmacists to provide comprehensive patient care for outpatients. The Clinical Pharmacy Specialist will also be responsible for counseling patients starting new intravenous …
Clinical Research Consent Writers are responsible for overseeing the authoring, development and overall quality assurance of the disease group’s consent documents submitted as part of the New Protocol Applications and any required consent amendments. The Consent Writers must work collaboratively and effectively manage priorities between projects and assigned pods with …
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 …
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 …
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 …
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 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 …
The Gastrointestinal (GI) Oncology Clinical Research Program at Dana-Farber Cancer Institute is seeking a Clinical Reserach Coordinator 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, pancreas, …
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 …
The Clinical Research Coordinator works within the 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 management of patient clinical information as …
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 …
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 …
The Specimen Based Clinical Research Coordinator work within the Pediatric Hematologic Malignancy clinical research program and support the research team in the overall conduct of the specimen-based clinical research studies using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The CRC will …
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 …
The CRC II supports 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 II will be responsible for the primary data collection and management of patient clinical information as it …
The Clinical Research Managers work within the clinical research program and manage the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of Principal Investigators and the Clinical Trials Office. The Clinical Research Manager, in collaboration with the program's physicians and research nursing …
