The Clinical Research Coordinator work within the Sarcoma 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 Thoracic 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 …
Under direct supervision of the Senior Clinical Research Financial Analyst, the Clinical Research Financial Analyst I (CRFA-I) 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 basic issues and problems and …
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 (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 Clinical Research Manager (CRM) will work within the GI 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 CRM, in collaboration with the program’s physicians …
The Research Project Manager II (RPM) is responsible for assigned day-to-day coordination and overall management of sponsor activities for assigned clinical trials; primarily multi-center, PI-initiated trials. Sponsor activities include coordinating trial startup and site startup activities, providing training to participating site research staff, regulatory submissions, safety event tracking and reporting, …
The Clinical Trials Office and the Center for RAS Therapeutics is looking for a Regulatory Coordinator (RC) to provide regulatory support for this new initiative. The RC will work under the direction of the Principal Investigator(s), and will directly report into the Clinical Trials Office to complete the regulatory requirements …
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 Division of Population Sciences is looking for a Research Assistant I (RAI) to work on a variety of cancer research projects that focus on both pediatric and adult patient populations. The Research Assistant’s efforts will primarily be focused on conducting medical record reviews, interacting with study participants in person …
The Research Assistant (RA) will work as part of the Palliative Care and Resilience (PCAR) research team within the Department of Supportive Oncology. PCAR collaborates closely with the Pediatric Advanced Care Team (PACT) to advance research and clinical initiatives that support palliative care and resilience for pediatric patients and their …
The Center for Early Detection and Interception of Blood Cancers at Dana-Farber Cancer Institute seeks a full-time Research Data Specialist (RDS) to help with data entry, data quality assurance, and data reporting tasks related to studies advancing understanding of multiple myeloma immunotherapy and multiple myeloma precursor states. The Research Data …
The Research Data Specialists 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 Data …
The Clinical Trials Office (CTO) and the Center for RAS Therapeutics is looking for a Research Data Specialist to provide research data entry, data collection, computing and database organization support for this new initiative. Other duties may include the examination, synthesis, and evaluation of medical records; the abstraction and recording …
The Research Data Specialists (RDS) will support the Neuro 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 …
The Thoracic Oncology Research Data Specialist 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. We are considering …
The Medical Oncology Division of Population Sciences wishes to hire a Research Project Manager I to help manage several oncology-related health services projects. The RPM will be responsible for day-to-day coordination and overall management of activities for assigned health outcome research protocols including multi-center, PI-initiated cancer care delivery projects. This …
The Research Project Manager I (RPM I) will support the Cohort Studies program under the auspices of the Principal Investigator(s) and Associate Director of Translational Research, in the areas of day-to-day coordination and overall management of the Dr. Parson’s Lab within the Department of Breast Oncology. The Parsons Laboratory fosters …
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 Sr. Medicare Coverage Analyst (MCA) is responsible for reviewing clinical research protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant study-related documents to create a coverage analysis/billing guide. The coverage analysis indicates which medical procedures/services maybe 'Routine Cost' and billable to patient insurance and which should be billed …
The Clinical Trials Office and the Center for RAS Therapeutics is looking for a Regulatory Coordinator (RC) to provide regulatory support for this new initiative. The RC will work under the direction of the Principal Investigator(s), and will directly report into the Clinical Trials Office to complete the regulatory requirements …
Read more about ""The Clinical Trials Office (CTO) and the Center for RAS Therapeutics is looking for a Research Data Specialist to provide research data entry, data collection, computing and database organization support for this new initiative. Other duties may include the examination, synthesis, and evaluation of medical records; the abstraction and recording …
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 …
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