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Associate Director / Director, Clinical Pharmacology

Treeline Biosciences · Watertown, Massachusetts, United States · On-site

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About Treeline Biosciences

Backed by GV.

About the role

This position is classified as exempt. The anticipated annual base salary range for candidates who will work in Watertown is $193,798 to $240,383. The final base salary offered to the successful candidate will be dependent upon several factors that may include but are not limited to the type and length of experience within the job, and other factors. Treeline Biosciences is a multi-state employer, and this salary range may not reflect positions that work in other cities or states.

What they're looking for

  • PhD, PharmD, or MD in Pharmacology, Pharmaceutical Sciences, or a related discipline
  • 5+ years of clinical pharmacology experience in the biotech or pharmaceutical industry, including leadership roles in clinical-stage development
  • Demonstrated expertise in clinical pharmacology strategy and study design from early development through registration
  • Deep understanding of PK/PD principles, modeling and simulation, and exposure–response analysis
  • Experience overseeing PK sample management, bioanalytical testing, and assay validation
  • Demonstrated cross-functional leadership and ability to integrate complex scientific data into strategic development decisions
More about this role

The Associate Director / Director of Clinical Pharmacology will serve as the scientific and strategic leader supporting Phase 1 studies and inclusion of clinical pharmacology assessments in early development and responsible for the design and execution of clinical pharmacology studies to inform clinical development. This individual will contribute to the planning, implementation, and delivery of studies supporting early- and late-stage clinical trials, lead data interpretation to guide development decisions, and collaborate closely with Clinical Development, Translational Medicine, Biomarkers, and Regulatory Affairs. The role also includes oversight of PK sample strategy, bioanalytical testing, and data integration to support pharmacokinetic (PK), pharmacodynamic (PD), and exposure–response analyses to support dose selection and therapeutic optimization.

  • Design and implementation clinical pharmacology strategies to Treeline’s programs to support IND, first-in-human, proof-of-concept, and registrational studies.
  • Develop and execute clinical pharmacology plans, including PK/PD modeling, dose selection, and exposure–response analyses.
  • Oversee collection, processing, and...

Read the full posting on Treeline Biosciences's site ↗

Clinical

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