Senior Director, Clinical Pharmacology — Remote

Travere Therapeutics

Columbus (OH)

On-site

USD 189,000 - 246,000

Full time

8 days ago

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Benefits offered by this job

Premium health benefits
Stock options
Retirement plans with company match
Generous paid time off

Job summary

Travere Therapeutics is seeking a Director of Clinical Pharmacology in San Diego. The role leads PK/PD strategy across programs, shapes dosing strategies, and partners with senior management and regulatory agencies to translate data into actionable program decisions.

The candidate will guide cross-functional teams, oversee studies, and contribute to regulatory filings while driving innovation in model-informed drug development for rare diseases.

Qualifications

  • Requires 6+ years of clinical pharmacology experience.
  • Experience leading PK/PD studies and modeling.
  • Experience with model-informed drug development (MIDD) strategies.

Responsibilities

  • Lead clinical pharmacology strategy and integrate PK/PD data into development plans.
  • Provide strategic guidance on dose, regimen, study design, and evidence needs.
  • Design and oversee PK/PD studies and modeling for early candidates.
  • Support regulatory submissions including briefs, INDs, CTAs, and NDAs.
  • Review protocols and reports for regulatory filings and address questions.
  • Develop clinical pharmacology documents such as protocols and CSRs.
  • Foster partnerships with R&D functions to align pharmacology plans with program needs.

Skills

PK/PD
Pharmacometrics
Leadership
Regulatory strategy
Dose selection
Cross-functional collaboration

Education

PhD or PharmD in Clinical Pharmacology

Job description

Travere Therapeutics is seeking a Director of Clinical Pharmacology in San Diego. The role leads PK/PD strategy across programs, shapes dosing strategies, and partners with senior management and regulatory agencies to translate data into actionable program decisions.

The candidate will guide cross-functional teams, oversee studies, and contribute to regulatory filings while driving innovation in model-informed drug development for rare diseases.

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