CellCarta is seeking a Clinical Study Specialist I to support site-level regulatory documentation, monitoring visits, and action item follow-up across oncology trials. You will act as a liaison between Project Management, Regulatory Affairs, and QA to ensure site initiation activities and essential document collection are executed with precision.
The role requires 2+ years in clinical research, familiarity with GCLP/GDP, and experience with eTMF and CTMS systems.
#J-18808-LjbffrOncology Clinical Study Specialist — SIV & Compliance in naperville at Unknown Company
This position is listed as full time and onsite.