CellCarta seeks a Clinical Study Specialist I to ensure operational success and integrity of site‑level regulatory documents, monitoring visits, initiation activities, and action item follow‑ups across oncology trials.
You will liaise with Project Management, Regulatory Affairs, and QA to drive audit readiness, manage SIVs, and oversee document collection for essential site submissions.
#J-18808-LjbffrOncology Clinical Ops Specialist — Site Start & Compliance in naperville at Unknown Company
This position is listed as full time and onsite.