Director, Clinical Pharmacology
Merck GroupAbout the role
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United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Your role: Director, Clinical Pharmacology position in Quantitative Pharmacology within the broader Clinical Measurement Sciences organization is a strategic, scientific, and cross-functional role, leading the Clinical Pharmacology (CP) Expert Team, responsible for developing and executing clinical pharmacology and Model Informed Drug Development (MIDD) strategies from the early to late-stage clinical development. This role represents the CP Expert Team to the global cross functional drug discovery and development project teams, in close collaboration with colleagues in Biostatistics, Data Sciences, Clinical Biomarkers and Diagnostics, Research, Clinical Development and other colleagues within the R&D organization.
The Director, Clinical Pharmacology provides strong leadership for integrating individual functional contributions, developing clinical pharmacology strategy in alignment with the overall clinical development plan, and executing the program strategy/plan. The scope includes programs from exploratory development (ED) through life cycle management, encompassing large and small molecule therapeutics/drug candidates across different therapeutic areas.
Key Accountabilities:
- Ensures that CP strategy is developed, aligned (with cross-functional development plans), endorsed and executed to support the indication, patient population, and phase of development while taking into account the competitive landscape
- Represent clinical pharmacology and promote MIDD with internal and external stakeholders
- Provides in-depth CP, PK and PK/PD advice and expertise and lead clinical pharmacology expert team and deliver on
- Dose and posology decisions, from FIH starting dose through submission and beyond
- Fit-for-purpose CP package including dose, dose regimen, and adjustment for specific conditions and specific populations, exposure-QTc assessment and immunogenicity assessment in collaboration with other function lines at appropriate stages of development
- Develop and execute MIDD strategies/plans in collaboration with pharmacometrics and other functions
- PK/PD data analysis, interpretation, and presentation
- Related sections of major clinical and regulatory documents (e.g. clinical protocols, IBs, CTDs, INDs, NDAs, IMPDs, briefing books)
- Contribute to due diligence projects, if needed
Location: Hybrid preferred, Remote possible with travel as required
Who you are:
Minimum Requirements
- 5+ years (Bio)pharmaceutical industry and/or postdoctoral experiences with clinical drug development experience
- Doctorate degree (PhD, PharmD or MD) rel
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