Jobs at The START Center for Cancer Research

Collect, transcribe, and submit clinical trial data into paper and electronic CRFs for investigational drug studies. Review patient records for completeness and accuracy, resolve queries, coordinate monitor visits, identify study labs for regulatory certification, and attend study meetings to support data quality and audit readiness.

Coordinate day-to-day conduct of early‑phase oncology clinical trials: screen patients, facilitate informed consent, collect and document data, educate patients on treatments/side effects, report serious adverse events, communicate with sponsors/CROs, and ensure GCP and regulatory compliance.

Configure and verify clinical trial protocols in the CTMS by translating Schedules of Assessments into configurable requirements. Build study tools (eligibility checklists, calendars, flow sheets), update Oncore data, coordinate study setup and activations, collaborate with SMEs and leadership, manage workflows, escalate risks, and ensure accurate clinical documentation to support Phase I oncology trial execution.

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.