Director, Clinical Pharmacology — Dosing Strategy Lead

Meet Life Sciences

California

Remote

USD 230,000 - 320,000

Full time

3 days ago
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Job summary

Meet Life Sciences Ltd. is seeking a Director, Clinical Pharmacology to shape dosing strategies and pharmacology plans across early development programs.

You will influence study design, interpret PK/PD and exposure–response data, and guide data-driven development decisions in collaboration with clinical teams. You will lead cross-functional efforts across development, operations, biostatistics, biomarkers, and regulatory, with remote US work and global regulatory interaction responsibilities.

Qualifications

  • 8+ years in clinical pharmacology and drug development.
  • Strong background in small-molecule development and ADME/PK–PD.
  • Hands-on non-compartmental PK analysis and interpretation.

Responsibilities

  • Lead clinical pharmacology strategy and provide input to development and study teams.
  • Deliver integrated interpretations of PK/PD, exposure–response, and biomarker data.
  • Drive dose selection and optimization to support study design decisions.
  • Manage the design and oversight of clinical pharmacology studies (ADME, interactions, food effect, bioavailability).
  • Analyze and interpret emerging clinical PK data and model-informed approaches.
  • Author and review clinical pharmacology sections for protocols and regulatory documents; support regulatory interactions.

Skills

Clinical pharmacology
PK/PD analysis
Model-informed DDD
Cross-functional collaboration

Education

Advanced scientific degree in clinical pharmacology
MS in a related field with 12+ years of experience

Job description

Meet Life Sciences Ltd. is seeking a Director, Clinical Pharmacology to shape dosing strategies and pharmacology plans across early development programs.

You will influence study design, interpret PK/PD and exposure–response data, and guide data-driven development decisions in collaboration with clinical teams. You will lead cross-functional efforts across development, operations, biostatistics, biomarkers, and regulatory, with remote US work and global regulatory interaction responsibilities.

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