The successful candidate should not only understand clinical pharmacology, DMPK, PopPK, PBPK, PK/PD, ADME, and safety data, but also be able to interpret these data critically and translate them into clear development decisions. • 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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