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- ...Trial Applications (CTA), modifications, and related documents in compliance with EU Clinical Trials Regulation (CTR), including follow-up and responding to Request For Information (RFI) Plan, prepare and collect documents for part I and part II and secure that national...
- ...create and drive a strategy Being solution oriented, responsible, good at details, pro-active, able to navigate easily in diverse set-up, self-motivated, independent working style. Advanced English language skills. About the affiliate and team The position...
