Oncology Clinical Trials Specialist I
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CellCarta is seeking a Clinical Study Specialist I to ensure site-level regulatory documentation, monitoring visits, and close-out activities are executed with precision. You will liaise with Project Management, Regulatory Affairs, and QA to maintain audit readiness across oncology trials.
The role requires 2+ years in clinical research, GCLP/GDP knowledge, and English fluency. It is a full-time, 100% onsite position within the Clinical Operations team.