Oncology Clinical Trials Specialist I

Il y a 2 jours

Antwerpen, Belgique CellCarta Temps plein 42 000 € - 65 000 € Contrat

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.