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Director, Clinical Pharmacology
Travere Therapeutics. Lead the design, development, and execution of clinical pharmacology strategies across clinical programs .
Posted 10/31/2026full-timeSan Diego • California • United StatesLead💰 $189,000 - $246,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Clinical Pharmacology, including the integration of Pharmacokinetics (PK) and Pharmacodynamics (PD) into clinical development plans. Proven ability to lead cross-functional teams and manage complex clinical pharmacology studies and regulatory submissions.
Highest-signal resume keywords
PhD Or PharmD In Clinical PharmacologyClinical Pharmacology ExpertiseModel-Informed Drug Development (MIDD)Project Leadership SkillsRegulatory Submission Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Pharmacokinetics (PK)Pharmacodynamics (PD)Dose-Escalation StudiesClinical Study ReportsInvestigator’s BrochuresClinical ProtocolsPharmacometricsBiopharmaceuticsEvidence IntegrationScientific Data Interpretation
Soft Skills
Excellent CommunicationCollaboration SkillsSelf-MotivatedLeadership SkillsAbility To Manage Multiple Tasks
Industry Keywords
Pharmaceutical DevelopmentBiotechnology DevelopmentRegulatory FilingsClinical Pharmacology StrategiesCross-Functional Project LeadershipClinical Development PlansDose And Regimen JustificationScientific RecommendationsClinical Pharmacology FunctionMultidisciplinary Teamwork
About the role
Key responsibilities & impact- Lead the design, development, and execution of clinical pharmacology strategies across clinical programs
- Integrate pharmacokinetics (PK), pharmacodynamics (PD), and drug-drug interaction assessments into clinical development plans
- Provide strategic guidance to clinical-stage project teams on dose, regimen, study design, and evidence needs
- Lead and oversee clinical pharmacology studies, including dose-escalation and PK/PD assessments and modeling
- Lead clinical pharmacology strategy and content for regulatory submissions, including briefing documents, INDs, CTAs, and NDAs
- Review clinical protocols and scientific reports for regulatory filings
- Identify potential gaps and prepare responses to regulatory questions
- Develop and independently author clinical pharmacology documents and sections, including clinical protocols, Investigator’s Brochures, and Clinical Study Reports
- Partner with Research, Bioanalytical, Clinical, Regulatory, Project Management, and other R&D functions
- Provide clinical pharmacology leadership at development milestones and portfolio decision points
- Contribute to advancing the Clinical Pharmacology function, capabilities, and practices
- Communicate clinical pharmacology recommendations to senior management, regulatory agencies, and external scientific peers
Requirements
What you’ll need- PhD or PharmD in Clinical Pharmacology, Pharmaceutical Sciences, or a related discipline, with 6+ years of relevant clinical pharmacology experience in pharmaceutical/biotechnology development or an equivalent drug-development setting
- Clinical pharmacology expertise in one or more therapeutic areas
- Experience integrating evidence across multiple development phases and partnering across relevant scientific disciplines
- Leadership in PK/PD, biopharmaceutics, and pharmacometrics across multiple projects
- Experience providing scientific and cross-functional project leadership
- Strong project leadership skills, including scope management, progress tracking, risk identification, and delivery against timelines
- Experience applying model-informed drug development (MIDD) strategies across development phases
- Ability to address questions on dose and regimen justification, labeling, and study design
- Ability to work effectively in a multidisciplinary team
- Ability to review, interpret, and present complex scientific data
- Excellent communication, collaboration, and project leadership skills
- Ability to manage multiple, complex tasks with competing timelines
- Self-motivated and able to independently manage responsibilities
- Ability to travel 10% domestically and internationally
- Ability to perform face-to-face work with colleagues and/or work onsite in San Diego
Benefits
Comp & perks- Premium health benefits for eligible employees and dependents
- Financial, work-life, and well-being offerings
- Wellness and employee support programs
- Life insurance
- Disability benefits
- Retirement plans with employer match
- Generous paid time off
- Short-term incentive compensation
- Long-term incentive compensation through company stock