These positions 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(s) and the DFCI Clinical Trials Office. The CRC will be responsible for the primary data collection and management of …
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 …
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 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 …
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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