Associate Director, Clinical Pharmacology – Remote Impact

Travere Therapeutics

Wichita (KS)

On-site

USD 150,000 - 195,000

Full time

14 days+
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Benefits offered by this job

Stock-based compensation
Comprehensive benefits

Job summary

Travere Therapeutics is seeking an Associate Director of Clinical Pharmacology in San Diego with remote collaboration. You will lead pharmacology strategies, integrate PK/PD across programs, and guide dose selection through early and late development.

You will provide input for IND/CTA/NDA filings, oversee pharmacology studies, and partner with regulatory and clinical teams to advance therapies for rare diseases.

Qualifications

  • PhD or PharmD required; relevant experience
  • Experience leading clinical pharmacology programs across development stages
  • Strong collaboration with regulatory, research and clinical teams
  • Experience with PK/PD modeling and MIDD approaches
  • Ability to communicate strategies to senior management and regulators

Responsibilities

  • Lead design and execution of clinical pharmacology strategy across development programs
  • Represent Clinical Pharmacology in cross-functional teams and regulatory interactions
  • Develop and oversee PK/PD studies and modeling to support dosing
  • Provide input for regulatory submissions (IND/CTA/NDA) and filings
  • Review protocols, ICH/CMC documents, and clinical study reports
  • Partner with Research, Regulatory, and Project Management to advance programs
  • Drive strategic pharmacology input at key decision points in development

Skills

PK/PD
Leadership
Regulatory submissions
Cross-functional collaboration
Pharmacometric

Education

PhD or PharmD

Job description

Travere Therapeutics is seeking an Associate Director of Clinical Pharmacology in San Diego with remote collaboration. You will lead pharmacology strategies, integrate PK/PD across programs, and guide dose selection through early and late development.

You will provide input for IND/CTA/NDA filings, oversee pharmacology studies, and partner with regulatory and clinical teams to advance therapies for rare diseases.

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