• Support strategic development planning, due diligence, partnering, and business development activities by identifying clinical pharmacology, DMPK, safety, and regulatory risks and proposing practical solutions. • Approximately at least 15 years of relevant experience in clinical pharmacology, DMPK, ADME, PK/PD, translational pharmacology, or regulatory-facing drug development; exceptional candidates with slightly less experience may be considered if they bring strong strategic and authority-facing expertise.
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