# Director Clinical Pharmacology at CSL

CSL is hiring a Director Clinical Pharmacology. Level rates it Little AI ●○○○; you can [apply on CSL](https://jobsbylevel.com/go/bed8d7d8-3649-4caf-8d9d-be9dd6324c88?utm_medium=ai-agent).

AI Level 1, AI centrality 32 out of 100. Americas, US-PA, King of Prussia, CSL Behring.

## Details

- Company: [CSL](https://jobsbylevel.com/companies/csl)
- AI level: AI Level 1 (score 32 out of 100)
- Location: Americas, US-PA, King of Prussia, CSL Behring
- Posted: October 15, 2026
- Apply: https://jobsbylevel.com/go/bed8d7d8-3649-4caf-8d9d-be9dd6324c88?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=director-clinical-pharmacology-at-csl-781de4

## Description

Director, Clinical Pharmacology Locations: King of Prussia, PA or Glattbrugg, Switzerland Work Arrangement: Hybrid – 3 days onsite Reports To: Senior Director, Clinical Pharmacology Lead About CSL CSL’s R&D organization is accelerating innovation to deliver greater impact for patients. Through a project-led structure and a strong focus on collaboration, we are building a future-ready organization that thrives in dynamic biotech ecosystems. Join CSL and become part of an agile team committed to developing innovative therapies that make a meaningful difference for patients around the world. The Opportunity CSL is seeking a Director, Clinical Pharmacology to provide clinical pharmacology and pharmacometrics expertise across a range of programs within its R&D portfolio. This individual will lead clinical pharmacology strategy, guide pharmacokinetic/pharmacodynamic (PK-PD) assessments, and drive the application of modeling and simulation to support drug development decisions throughout the clinical development lifecycle. The successful candidate will operate with a high degree of independence, bringing strong scientific expertise, innovative thinking, and a solution-oriented approach to cross-functional collaboration. Working closely with clinical development, research, translational science, biostatistics, and other R&D partners, the Director will ensure the integration of clinical pharmacology strategies into global development plans. This role will also serve as a key clinical pharmacology representative in regulatory interactions, contributing to submission documents, regulatory responses, and discussions with health authorities to support successful development and registration of therapies. Main Responsibilities and Accountabilities Clinical Pharmacology Strategy: Lead clinical pharmacology and PK-PD strategies for assigned programs across the R&D portfolio, partnering with pharmacometricians, clinical program directors, clinical scientists, biostatisticians, and other cross-functional colleagues. Clinical Study Design and Oversight: Lead the design of clinical pharmacology studies and relevant protocol sections across all stages of drug development. Provide scientific oversight of study implementation in collaboration with Clinical Development, Clinical Safety, and Clinical Research Operations. Pharmacokinetic and PK-PD Analyses: Plan and implement appropriate pharmacokinetic and pharmacodynamic analyses, including non-compartmental analysis and other relevant analytical approaches, to inform clinical development decisions. Data Interpretation and Reporting: Lead the review and interpretation of clinical pharmacology study results, ensuring high-quality presentation and documentation in clinical study reports, scientific publications, and related study materials. Cross-Functional Collaboration: Represent clinical pharmacology and pharmacometrics on clinical development teams, ensuring alignment across functions and integration of clinical pharmacology strategies into global development plans. Modeling and Simulation: Apply innovative pharmacometric methodologies, including modeling and simulation, to integrate pharmacokinetics, pharmacodynamics, patient characteristics, and disease states. Use these insights to inform dose selection, study design, and development strategies throughout the clinical development lifecycle. Regulatory Strategy and Submissions: Provide clinical pharmacology expertise for protocols, Investigator’s Brochures, regulatory submissions, product labeling, and other regulatory documentation. Lead the development of clinical pharmacology strategies and written responses to health authority questions, and contribute to regulatory meetings and filing activities as needed. Research and Translational Science Support: Partner with Research and Translational Science teams to develop preclinical PK-PD knowledge supporting early clinical development strategies and appropriately incorporate pharmacology and

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