Associate Director, Pharmacokinetics (PK) — CSL Behring

CHF 68'000 - 103'000
CSL Behring · Glattbrugg (ZH)
Categoria: Sanità Contratto: full-time Salario: CHF 68'000 - 103'000
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Location
Glattbrugg
Contract
full-time
Posted
35 days ago
SalaryCHF 68'000 - 103'000

Role overview

CSL's R&D organization is accelerating innovation to deliver greater impact for patients.

With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems.

Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.

Position Description Summary: The Associate Director PK is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK), toxicokinetic (TK), strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas.

Expert will lead a team of Principle and Senior PK Scientists to ensure effective and consistent approaches for IND-enabling PK strategies and studies.

Main Responsibilities: Strategic Leadership

  • Lead the design and execution of pharmacokinetic (PK) and toxicokinetic (TK) strategies.
  • Provide scientific leadership across drug discovery, nonclinical, and development programs.
  • Ensure alignment of PK/TK strategies with overall program goals across multiple therapeutic areas.

Team Management

  • Supervise and mentor a team of Principal and Senior PK Scientists.
  • Foster a collaborative and high-performance team environment.

Main responsibilities

  • Main Responsibilities: Strategic Leadership
  • Lead the design and execution of pharmacokinetic (PK) and toxicokinetic (TK) strategies.
  • Provide scientific leadership across drug discovery, nonclinical, and development programs.
  • Ensure alignment of PK/TK strategies with overall program goals across multiple therapeutic areas. Team Management
  • Supervise and mentor a team of Principal and Senior PK Scientists.
  • Foster a collaborative and high-performance team environment.
  • Guide team members in developing and implementing IND-enabling PK strategies. Study Oversight and Execution
  • Oversee the planning, execution, and interpretation of PK/TK studies.
  • Ensure scientific rigor and regulatory compliance in studies conducted at external CROs
  • Troubleshoot and resolve issues related to study design, data interpretation, and timelines. Cross-Functional Collaboration

Key requirements

  • and Experience Requirements:
  • Ph.D. in a Life Sciences discipline such as Pharmacokinetics, Systems Pharmacology, Pharmacometrics, Biomedical Engineering, or a related field.
  • 8+ years of industry experience in PK/PD, PBPK.
  • Proficiency in relevant software for PK/PD, PBPK.
  • Strong understanding of ADME, pharmacology, and translational science.
  • Excellent 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.

Company and context

  • CSL's R&D organization is accelerating innovation to deliver greater impact for patients.
  • With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems.
  • Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.
  • Position Description Summary: The Associate Director PK is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK), toxicokinetic (TK), strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas.
  • The Sr.
  • Expert will lead a team of Principle and Senior PK Scientists to ensure effective and consistent approaches for IND-enabling PK strategies and studies.
  • Excellent communication and stakeholder engagement skills, with the ability to influence at all levels of the organization.
  • About CSL Behring CSL Behring is a global biotherapeutics leader driven by our promise to save lives.
  • Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
  • We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

Additional details

  • Ensure alignment of PK/TK strategies with overall program goals across multiple therapeutic areas.
  • Guide team members in developing and implementing IND-enabling PK strategies. Study Oversight and Execution
  • Troubleshoot and resolve issues related to study design, data interpretation, and timelines. Cross-Functional Collaboration
  • Qualifications and Experience Requirements:

Notes and original content

  • Team Management
  • Guide team members in developing and implementing IND-enabling PK strategies.
  • Study Oversight and Execution
  • Troubleshoot and resolve issues related to study design, data interpretation, and timelines.
  • Cross-Functional Collaboration
Apply now
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Company
CSL Behring · Glattbrugg
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