VP, Regulatory Diligence & Strategy

Travere Therapeutics; Denver (CO); On-site; USD 285,000 - 385,000; Full time

Job summary

Travere is seeking a Vice President, Regulatory Strategy Diligence to lead the Regulatory Due Diligence team for external opportunities. The role evaluates licensing, acquisition, partnership, and external innovation opportunities, with focus on regulatory readiness and risk mitigation across clinical and manufacturing aspects.

The successful candidate will partner with BD, Regulatory, Quality, and Legal to inform strategic decisions and post-deal integration, with travel 10–20% and

Qualifications

• Master's or PhD (preferred) in pharmaceutical sciences, biological sciences, engineering, chemistry, or related field.
• 15+ years in pharma/biotech with regulatory and development experience focused on business development.
• 8+ years of people management and leadership experience.
• Experience interacting with executive leadership in strategic transactions.
• Experience in biotech/pharma with both biologics and small molecules is preferred.

Responsibilities

• Lead regulatory due diligence for licensing, acquisition, partnership, and external opportunities.
• Assess regulatory readiness, develop risk mitigations, and communicate assumptions to leadership.
• Own regulatory risk assessment and recommendations for each opportunity.
• Evaluate CMC, manufacturing, analytics, technology transfer, and lifecycle plans.
• Lead input into term sheets, agreements, and governance related to regulatory matters.
• Prepare diligence reports, risk registers, and executive presentations.

Skills

Regulatory strategy

Due diligence leadership

Executive communication

Cross-functional collaboration

Project management

Regulatory submissions

Risk assessment

Strategic thinking

Education

Master's or PhD in pharmaceutical sciences or related

Job description

Travere is seeking a Vice President, Regulatory Strategy Diligence to lead the Regulatory Due Diligence team for external opportunities. The role evaluates licensing, acquisition, partnership, and external innovation opportunities, with focus on regulatory readiness and risk mitigation across clinical and manufacturing aspects.

The successful candidate will partner with BD, Regulatory, Quality, and Legal to inform strategic decisions and post-deal integration, with travel 10–20% and