Director Pharmacokinetics

Vor 3 Tagen


Opfikon, Schweiz CSL Vollzeit

Description Summary:The PK/QSP Lead is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK), toxicokinetic (TK), physiologically-based pharmacokinetic (PBPK), and quantitative systems pharmacology (QSP) modeling strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas. Main Responsibilities: Strategic Leadership & Scientific Expertise​Lead the development and execution of integrated PK, PBPK, and QSP modeling strategies across multiple therapeutic programs.​Serve as the subject matter expert (SME) in modeling and simulation, advising project teams on optimal study design, dose selection, and risk assessment.​Champion model-informed drug development (MIDD) approaches to enhance translational understanding and regulatory confidence.​PK and Model Development​Lead the design and execution of nonclinical PK and TK studies to support research and IND-enabling packages.​Lead the design and execution of PBPK and QSP modeling strategies across multiple programs.​Cross-Functional Collaboration​Act as Sr. PK/QSP lead on TA teams.​Collaborate closely with Research, Nonclinical development functions, Clinical Development and Clinical Pharmacometrics to ensure alignment of Pharmacokinetic and modeling strategies with program goals.​Participate in cross-functional project teams, providing scientific input and modeling insights to guide key development decisions.​Provide expert input into due diligence for in-licensing or partnership opportunities.​Regulatory & Documentation​Contribute to and review Nonclinical Pharmacokinetic sections for submission documents.​Prepare and review modeling reports and regulatory documents.​Innovation & Continuous Learning​Stay abreast of emerging trends, technologies, and regulatory expectations in PK, PBPK, and QSP modeling.​Contribute to scientific publications, conference presentations, and internal knowledge-sharing initiatives.​Team Leadership:​Lead and mentor a team of Principal and Sr. scientists.​Foster a culture of scientific excellence, innovation, and continuous learning. Qualifications and Experience Requirements: Ph.D. in Pharmacokinetics, Systems Pharmacology, Pharmacometrics, Biomedical Engineering, or a related field.​10+ years of pharmaceutical industry experience in PK/PD, PBPK, and/or QSP modeling.​Proven track record of applying modeling to support drug development and regulatory submissions.​Proficiency in modeling software for PK/PD, PBPK, QSP​Strong understanding of ADME, pharmacology, and translational science.​Excellent communication, leadership, and project management skills.​Experience with omics data integration, machine learning, or AI-enhanced modeling is a plus.​Ability to manage multiple projects and timelines.​Experience across multiple therapeutic areas and modalities is highly desirable.​ Our Benefits We encourage you to make your well-being a priority. It’s important and so are you.



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