VP, Regulatory Diligence & Strategy

Travere Therapeutics; Providence (RI); On-site; USD 285,000 - 385,000; Full time

Benefits offered by this job

Premium health benefits

Employer matching retirement plans

Generous paid time off

Job summary

Travere Therapeutics seeks a Vice President, Regulatory Strategy Diligence to lead regulatory due diligence for external opportunities. You will assess licensing, acquisitions, and partnerships, translating complex data into executive recommendations.

The role requires deep regulatory development expertise across small molecules, biologics, and gene therapies, with cross-functional collaboration across BD, Legal, QA, and Clinical teams. Onsite in San Diego, travel up to 20%.

Qualifications

• 15+ years in pharma/biotech with regulatory and BD focus.
• 8 years of people management and leadership.
• Experience with biologics and small molecules preferred.
• Strong GMP and regulatory submission knowledge.
• Ability to translate complex data for senior executives.

Responsibilities

• Lead regulatory due diligence for licensing and acquisitions.
• Evaluate drug/device regulatory development and timelines.
• Own integrated regulatory risk assessment for opportunities.
• Assess CMC, manufacturing, analytics, and lifecycle plans.
• Review CRO/CMO capabilities and readiness.
• Collaborate with BD, Legal, QA, and Ops teams.
• Prepare diligence reports, risk registers, and exec decks.
• Contribute to term sheets, quality and supply agreements.
• Establish enterprise regulatory diligence standards.
• Advise leadership on regulatory considerations for transactions.
• Travel 10–20% domestically and internationally.

Skills

Regulatory strategy

Due diligence

Cross-functional leadership

Executive communication

GMP/regulatory knowledge

Education

Advanced degree in pharmaceutical sciences

Job description

Travere Therapeutics seeks a Vice President, Regulatory Strategy Diligence to lead regulatory due diligence for external opportunities. You will assess licensing, acquisitions, and partnerships, translating complex data into executive recommendations.

The role requires deep regulatory development expertise across small molecules, biologics, and gene therapies, with cross-functional collaboration across BD, Legal, QA, and Clinical teams. Onsite in San Diego, travel up to 20%.