We are seeking a senior Clinical Pharmacology expert who can combine deep pharmaceutical industry experience with a strong understanding of regulatory authority expectations. • 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. • Demonstrated experience in pharmaceutical or biotech drug development, ideally covering several stages from early development through IND/CTA and later-stage regulatory planning. • Experience with DMPK, ADME, PK/PD, PopPK, PBPK, exposure–response, dose selection, drug interaction strategy, formulation-related clinical pharmacology, safety considerations, and special population assessments.
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