Remote Director of Clinical Pharmacology & Development

Travere Therapeutics; San Diego (CA); On-site; USD 189,000 - 246,000; Full time

Job summary

Travere Therapeutics is seeking a Director of Clinical Pharmacology in San Diego to lead strategy across clinical programs, integrating PK/PD data and guiding dose and design decisions. Collaboration with regulatory, research, and development teams will shape portfolio decisions and regulatory filings.

The role requires a PhD or PharmD with 6+ years of pharmacology experience, leadership skills, and strong communication to translate complex data into actionable program guidance.

Qualifications

• PhD or PharmD in Clinical Pharmacology, Pharmaceutical Sciences, or related field with 6+ years of relevant experience.
• Leadership in PK/PD, biopharmaceutics, and pharmacometrics across multiple projects.
• Experience providing cross-functional project leadership and influencing decisions.
• Experience applying model-informed drug development (MIDD) strategies across development phases.
• Experience preparing regulatory submissions and scientific documents.

Responsibilities

• Lead the design, development, and execution of clinical pharmacology strategies across programs.
• Provide strategic guidance to project teams on dose, regimen, study design, and evidence needs.
• Oversee design and implementation of PK/PD studies and modeling for early candidates.
• Support regulatory submissions with clinical pharmacology content and responses to questions.
• Review protocols and reports for regulatory filings and address potential gaps.
• Author clinical pharmacology documents such as protocols, Investigator's Brochures, and study reports.

Skills

Leadership

PK/PD

Drug Development

Regulatory Strategy

Education

PhD or PharmD in Clinical Pharmacology

Job description

Travere Therapeutics is seeking a Director of Clinical Pharmacology in San Diego to lead strategy across clinical programs, integrating PK/PD data and guiding dose and design decisions. Collaboration with regulatory, research, and development teams will shape portfolio decisions and regulatory filings.

The role requires a PhD or PharmD with 6+ years of pharmacology experience, leadership skills, and strong communication to translate complex data into actionable program guidance.