Additionally, the design, drafting, and review of clinical trial protocols, amendments, and study-related documents fall within your scope of responsibility. * You hold an advanced degree (PhD, MD, PharmD, or equivalent) in life sciences, medicine, or a related field paired with significant experience in clinical development within the pharmaceutical or biotech industry, ideally including exposure to advanced therapy medicinal products (ATMPs) and/or CAR-T therapies. * You have a proven track record in protocol development, regulatory submissions (IND, CTA, BLA, MAA), and clinical data interpretation, and are recognized as an expert in the end-to-end process of clinical data generation, from protocol design through to final reporting
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