Research Associate I
Current• Understand and interpret clinical trial study protocol, clinical trial agreement (CTA), sponsor budget document, Investigator brochure (IB), Informed consent (ICF), pharmacy manual, Laboratory manual, coverage analysis workbook and site budget documents to design and develop calendars, site budgets and coverage analysis with knowledge of using CTMS software tool (Oncore).• Trained Coverage Analyst, to interpret and use National Coverage Determinations (NCDs) and Local Coverage Determinations (LCDs), Medicare's Clinical Trial Policy, peer-reviewed publications to determine which services indicated in the clinical trial protocol are billable charges and which should be deemed as non-covered research only services.• Assists in drafting updates or revisions to current organizational policies with coverage analysis service and any procedures pertaining to Coverage Analysis and Medicare compliant billing.• Collaborate with reporting manager directly to diligently complete all the tasks, ensuring high quality in all the assigned services.•Working directly with clinical trial sites to expedite the trials' activities during the phases of site selection and site initiation.