Remote VP, Regulatory Strategy & Diligence

Travere Therapeutics; New York (NY); On-site; USD 285,000 - 385,000; Full time

Benefits offered by this job

Premium health

Financial benefits

Work-life programs

Life insurance

Disability

Retirement with match

Paid time off

Job summary

Travere Therapeutics in San Diego is seeking a Vice President, Regulatory Strategy Diligence to lead regulatory due diligence for external business development opportunities. You will evaluate licensing, acquisition, partnership and external innovation opportunities, identifying regulatory risks and developing mitigation strategies across CMC, nonclinical, and clinical development.

The ideal candidate brings deep regulatory expertise across small molecules, biologics, and gene therapy, with

Qualifications

• Master's or PhD preferred in pharmaceutical sciences, biological sciences, engineering, chemistry, chemical engineering, or related field.
• Experience with regulatory development and business development focusing on clinical, manufacturing and technical operations.
• Proven leadership and ability to interact with senior management.

Responsibilities

• Lead regulatory due diligence for licensing, acquisition, partnership and external innovation opportunities.
• Assess regulatory development across clinical and commercial assets, including CMC and manufacturing.
• Own integrated regulatory risk assessment and communicate assumptions, dependencies and mitigations.
• Prepare diligence reports, risk registers, and executive presentations.
• Contribute to term sheets, agreements and governance documents.

Skills

Regulatory strategy

Due diligence

Executive communication

Cross-functional leadership

GMP knowledge

Travel willingness

Education

Master's or PhD preferred in relevant scientific field

Job description

Travere Therapeutics in San Diego is seeking a Vice President, Regulatory Strategy Diligence to lead regulatory due diligence for external business development opportunities. You will evaluate licensing, acquisition, partnership and external innovation opportunities, identifying regulatory risks and developing mitigation strategies across CMC, nonclinical, and clinical development.

The ideal candidate brings deep regulatory expertise across small molecules, biologics, and gene therapy, with