Teams at The START Center for Cancer Research

Research and map clinical research financials from CTMS reports, reconcile site expenses, support sponsor/CRO invoicing, collaborate with accounting and clinical teams, and improve mapping and reconciliation processes to ensure accurate sponsor billing and revenue capture.

Prepare and submit regulatory documents (IRB, FDA, IBC) for oncology clinical studies, draft informed consents, maintain Investigator Site Files, act as point of contact with Sponsors/CROs and regulatory bodies, track activities in regulatory systems, and respond to inquiries and status requests.

Develop, implement, and maintain clinical trial budgets and financial guidelines. Review protocols, perform coverage analysis, prepare and negotiate budgets and contract payment terms, and coordinate with clinical teams and sponsors to ensure billing compliance.