VP, Regulatory Due Diligence & Strategy

Travere Therapeutics; Columbus (OH); Hybrid; USD 285,000 - 385,000; Full time

Benefits offered by this job

Premium health benefits

Retirement plans with employer match

Generous paid time off

Job summary

Travere Therapeutics is seeking a Vice President, Regulatory Strategy Diligence to lead regulatory due diligence for business development opportunities, including licensing, acquisitions and partnerships.

You will evaluate regulatory readiness across clinical and commercial assets, identifying risks and mitigating strategies, and collaborate with BD, Clinical, Legal and Quality leaders to guide post-deal integration.

Qualifications

• 15+ years in pharma/biotech with regulatory and business development focus.
• Experience leading regulatory diligence and asset evaluations.
• Strong GMP knowledge and regulatory guidance understanding.
• Proven ability to communicate complex regulatory/technical info to executives.

Responsibilities

• Lead regulatory due diligence for licensing, acquisitions, partnerships and external innovation opportunities.
• Assess regulatory development paths, CMC, pediatrics and agency feedback for opportunities.
• Produce diligence reports, risk registers, and executive presentations.
• Collaborate with BD, Clinical, Regulatory, Quality, Legal and Operations teams.

Skills

Regulatory strategy

Due diligence

Leadership

Executive communication

Pharmaceutical/biotech

Education

Master's or PhD in pharmaceutical sciences or related

Tools

Regulatory tools and frameworks

Job description

Travere Therapeutics is seeking a Vice President, Regulatory Strategy Diligence to lead regulatory due diligence for business development opportunities, including licensing, acquisitions and partnerships.

You will evaluate regulatory readiness across clinical and commercial assets, identifying risks and mitigating strategies, and collaborate with BD, Clinical, Legal and Quality leaders to guide post-deal integration.