VP, Regulatory Due Diligence & Strategy (Remote)

Travere Therapeutics; Minneapolis (MN); Remote; USD 285,000 - 385,000; Full time

Benefits offered by this job

Premium health benefits

Stock options

Generous paid time off

Job summary

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

You will assess clinical/commercial assets, identify material regulatory risks, and collaborate with BD, Clinical, Regulatory, Quality, and Legal teams to support strategic decisions.

Qualifications

• 15+ years of relevant experience in pharmaceutical or biotechnology industries with regulatory development and business development focus.
• Experience leading regulatory diligence for licensing, acquisitions, partnerships, or external alliances.
• Strong understanding of GMP, regulatory expectations, clinical trial design, analysis, and lifecycle management.
• Ability to translate complex regulatory/technical information into clear risks, recommendations, timelines, and mitigations for senior management.

Responsibilities

• Lead regulatory due diligence for licensing, acquisition, partnership, and external innovation opportunities.
• Evaluate regulatory development across product development, pediatrics, agency feedback, and risks with timelines.
• Own integrated regulatory risk assessment and communicate assumptions, dependencies, timelines, and mitigations.

Skills

Regulatory strategy

Due diligence

Leadership

Cross-functional collaboration

Executive communication

Education

Master's or PhD preferred

Job description

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

You will assess clinical/commercial assets, identify material regulatory risks, and collaborate with BD, Clinical, Regulatory, Quality, and Legal teams to support strategic decisions.