Oncology Clinical Study Specialist — SIV & Compliance

Caprion Biosciences Inc.

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-Ljbffr Caprion Biosciences Inc.

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Vacancy posted 2 days ago

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