Additionally, the design, drafting, and review of clinical trial protocols, amendments, and study-related documents fall within your scope of responsibility. * You integrate translational insights, biomarkers, and clinical endpoints into development plans and work effectively across a matrix environment of internal , external , and partners to ensure alignment from early research through late-stage clinical development. * 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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