Associate Director Translational Pharmacokinetics and Pharmacokinetic/Pharmacodynamic

Role Summary:
The Associate Director role supports PK and PK/PD requirements for early-stage drug discovery and IND projects.

Responsibilities:
- Serve as a subject matter expert on preclinical PK/PD and guide design of preclinical PK/pharmacology studies.
- Provide input and oversight for preclinical in vivo studies.
- Coordinate with and influence internal scientific teams to develop and execute project PK strategies.
- Manage nonclinical PK studies.
- Communicate project team queries, expectations, and timelines to management.
- Conduct and report PK/PD analyses based on preclinical study data.
- Work with Toxicology, Pathology, Clinical Pharmacology, and Quantitative Pharmacology teams to deliver data and regulatory documents supporting project progression.
- Maintain current knowledge of scientific literature, regulatory guidance, and PK/PD best practices.

Qualifications/Requirements:
- PhD in Pharmacology, Pharmacokinetics, Biology/Molecular Biology, or Biochemistry with 8–10+ years of relevant biotech/pharma experience.
- Deep theoretical and applied understanding of PK/PD to interpret therapeutic protein pharmacology/biology; experience with other modalities (e.g., siRNA, CRISPR-based therapeutics, cell therapies) is highly beneficial.
- Proven ability to plan, coordinate, lead PK and/or PK/PD studies, and analyze related data.
- Familiarity with PK/PD tools (e.g., WinNonLin), data visualization and AI software; experience writing scientific reports and regulatory summaries.

Application:
- Apply now.