You demonstrate comprehensive expertise across the clinical data lifecycle—working backwards from the desired final readouts to plan early for the necessary data, overseeing capture, coordinating cleaning and integrity checks, and obtaining study results in collaboration with biostatistics, programming, data management, and medical monitoring teams—ensuring outputs that are decision-ready for regulatory and clinical use. * A key focus lies in ensuring the generation of high-quality clinical data and supporting the preparation of regulatory submissions (e.g., IND, CTA, BLA, MAA). * As an integral team member of Clinical Drug Development, you communicate complex scientific data clearly and effectively in English, both in writing and speaking, and leadership by coaching,
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