The Senior Director, Cardiovascular and Metabolic Diseases, Clinical Pharmacology Modeling and Simulation will lead the end-to-end application of Model-Informed Drug Development (MIDD) across the drug development lifecycle.
\nThe role sits within the newly established Clinical Pharmacology and Quantitative Medicine (CPQM) organisation, which aims to be a centre of excellence in MIDD by integrating clinical pharmacology, digital medicine, translational imaging, and mechanistic/systems modelling.
\nMain responsibilities and accountabilities include:
\nThe ideal candidate will have a PhD, MD, or PharmD, 8+ years of industry experience in clinical pharmacology, modelling/simulation, and drug development, and experience in pharmacometrics and its application to clinical questions in drug development.
\nThe salary range for this position is $222,750 to $371,250 per year, depending on location and experience. The company offers a comprehensive benefits program, including health care and other insurance benefits, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.
\nJob Data by YubHub.
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\nThis role sits within the newly established Clinical Pharmacology and Quantitative Medicine (CPQM) organisation, which aims to be a centre of excellence in Model‑Informed Drug Development (MIDD) by integrating clinical pharmacology, digital medicine, translational imaging and mechanistic/systems modelling.
\nYou will lead the end‑to‑end application of MIDD across the drug development lifecycle - from first‑in‑human studies through filing and lifecycle management - and provide clinical pharmacology strategy and evidence‑generation input.
\nMain responsibilities and accountabilities include:
\nDevelop and implement robust MIDD & ClinPharm evidence strategies to de risk and accelerate RIIRU programs.
\nDraft and review clinical pharmacology regulatory content to support timely approvals and optimal labelling.
\nWork closely with CPQM peers and cross functional partners.
\nRaise GSK’s profile in MIDD, clinical pharmacology, QSP and AI/ML integration through publications, conference presentations and active participation in scientific and regulatory fora.
\nBasic Qualifications:
\nPreferred Qualifications:
\nSkills Drug Design, Drug Development, Drug Discovery Process, Drug Discovery Research, Medication Safety, Molecular Modeling, Pharmaceutical Regulatory Compliance, Pharmaceutical Sciences, Pharmacodynamics, Pharmacokinetics, Pharmacology, Pharmacometrics, Pharmacovigilance, Study Design, Target Validation
\nJob Data by YubHub.
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