Associate Director, Pharmacology

What You Will Do

• Lead PK/PD data analysis and modeling activities, applying mechanistic and population modeling approaches using tools such as Phoenix WinNonlin, NONMEM, and related platforms.


• Apply quantitative and statistical methods to support non‑clinical and early‑phase clinical pharmacology programs.


• Contribute to regulatory interactions and submissions, including INDs, BLAs, MAAs, Investigator’s Brochures, briefing packages, and responses to agency queries.


• Communicate complex clinical pharmacology concepts clearly and effectively to cross‑functional and external stakeholders.


• Provide scientific leadership in matrixed teams, driving pharmacology strategy, problem‑solving, and decision‑making across programs.


• Lead the analysis, integration, and reporting of clinical pharmacology data to inform dose selection and study design.


• Design and implement pharmacology plans and ensure best practices across project teams.


• Partner with clinicians and statisticians to optimise dosing strategies and clinical study designs.


• Oversee study‑level pharmacology activities, including protocol and SAP development, execution, and reporting.


• Drive the design and execution of Model‑Informed Drug Development (MIDD) strategies.


• Represent Pharmacology on global program teams, clinical sub teams, and other multifunctional groups. • Mentor and coach junior colleagues and team members. • Stay current with scientific literature, regulatory guidelines, and internal SOPs.