Associate Director, Clinical Pharmacology - Remote PK/PD Strategy

Travere Therapeutics

Boston (MA)

Hybrid

USD 150,000 - 195,000

Full time

14 days+
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Job summary

Travere Therapeutics in San Diego seeks an Associate Director, Clinical Pharmacology to design, lead, and implement clinical pharmacology strategies across programs. You will communicate key pharmacology concepts to senior management, regulatory agencies, and external peers, and act as a liaison to other R&D functions.

The role requires a PhD or equivalent (or PharmD with 8+ years), demonstrated PK/PD leadership, dose and regimen guidance, and experience with MIDD.

Qualifications

  • Ph.D. or equivalent required; PharmD with 8+ years also acceptable.
  • Leadership of PK/PD, Biopharmaceutics, and pharmacometrics across programs.
  • Experience across multiple development phases and disease areas.

Responsibilities

  • Lead the development and execution of clinical pharmacology strategy for assigned development programs, integrating PK/PD and DDI assessments.
  • Represent Clinical Pharmacology and provide support to clinical stage project teams.
  • Design and oversee PK/PD studies to ensure optimal dosing strategies and evidence generation.
  • Provide input for regulatory submissions (IND, CTA, NDA) and related documents.
  • Review protocols and reports for regulatory filings and anticipate questions.
  • Collaborate with Research, Regulatory, and other R&D functions.
  • Play a key role in delivering strategic clinical pharmacology input at key decision points.

Skills

PK/PD
Biopharmaceutics
Pharmacometrics
Leadership
Project management
Communication

Education

PhD or equivalent
PharmD with 8+ years

Job description

Travere Therapeutics in San Diego seeks an Associate Director, Clinical Pharmacology to design, lead, and implement clinical pharmacology strategies across programs. You will communicate key pharmacology concepts to senior management, regulatory agencies, and external peers, and act as a liaison to other R&D functions.

The role requires a PhD or equivalent (or PharmD with 8+ years), demonstrated PK/PD leadership, dose and regimen guidance, and experience with MIDD.

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