VP, Regulatory Strategy & Due Diligence

Travere; United States; Remote; USD 250,000 - 350,000; Full time

Job summary

Travere Therapeutics is seeking a Vice President, Regulatory Strategy Diligence to lead regulatory due diligence for strategic opportunities. You will evaluate regulatory readiness, CMC considerations and risk across assets, coordinating with BD, Clinical, Regulatory and Quality teams to guide investment decisions.

Ideal candidates have extensive regulatory development experience in small molecules, biologics, ATMPs and companion diagnostics, with strong business judgment and confidential

Qualifications

• Master's or PhD preferred in pharmaceutical sciences or related field.
• 15+ years of relevant experience in pharma/biotech with BD focus including clinical, manufacturing and technical operations.

Responsibilities

• Lead regulatory due diligence for licensing, acquisition, partnerships and external innovation opportunities.
• Assess readiness risks for clinical and commercial assets and identify mitigation strategies.
• Collaborate with BD, Clinical, Regulatory, Quality, Legal and Technical Operations to support decisions.
• Prepare diligence reports, risk registers and executive presentations.
• Contribute to term sheets, definitive agreements and regulatory diligence standards.

Skills

Regulatory strategy

Due diligence

Cross-functional collaboration

Risk assessment

Regulatory affairs

Education

Master's degree or PhD in pharmaceutical sciences

Job description

Travere Therapeutics is seeking a Vice President, Regulatory Strategy Diligence to lead regulatory due diligence for strategic opportunities. You will evaluate regulatory readiness, CMC considerations and risk across assets, coordinating with BD, Clinical, Regulatory and Quality teams to guide investment decisions.

Ideal candidates have extensive regulatory development experience in small molecules, biologics, ATMPs and companion diagnostics, with strong business judgment and confidential