• Develop integrated clinical pharmacology, DMPK, ADME, PK/PD, and model-informed development plans to support dose selection, study design, safety assessment, and regulatory submissions. • Interpret clinical and nonclinical pharmacology, PK, safety, exposure–response, and modeling data and translate them into pragmatic, regulatorily defensible development decisions. • Support strategic development planning, due diligence, partnering, and business development activities by identifying clinical pharmacology, DMPK, safety, and regulatory risks and proposing practical solutions. • Collaborate closely with clinical development, regulatory affairs, CMC, nonclinical, safety, biomarker, and business development colleagues. • Proven ability to interpret clinical and nonclinical pharmacology, PK, safety, exposure–response, and modeling data and translate them into clear, pragmatic, and ...
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