Global Regulatory Affairs SVP — Strategy & Leadership

Vir-Biotechnology; San Francisco (CA); On-site; USD 350,000 - 400,000; Full time

Benefits offered by this job

Bonus and equity

Health and welfare plans

401K match

Job summary

Vir Biotechnology, Inc. seeks a Senior Vice President, Regulatory Affairs to lead the global Regulatory Affairs organization from preclinical through lifecycle management, including late-stage HDV program filings and Health Authority interactions.

The role is based in San Francisco with in-office expectations. Ideal candidate holds an advanced degree (PhD/MD/PharmD) and 15+ years of regulatory experience, with a proven track record in FDA/EMA engagements and major submissions.

Qualifications

• Advanced scientific or medical degree required.
• 15+ years of Regulatory Affairs experience with leadership impact.
• Experience leading global regulatory submissions and approvals.

Responsibilities

• Lead Vir Bio's global Regulatory Affairs organization and set vision, strategy, structure, and capabilities.
• Provide strategic counsel to executive leadership and influence portfolio decisions.
• Define and execute global regulatory strategies across development stages.
• Oversee regulatory interactions with Health Authorities (FDA/EMA) and drive successful outcomes.
• Lead filing readiness, submission planning, and post-marketing commitments for major applications.
• Assess regulatory risks and opportunities to inform development strategy and planning.

Skills

Regulatory leadership

Global regulatory strategy

FDA interactions

BLA submissions

Biotech/pharma

Team leadership

Regulatory strategy

Cross-functional collaboration

Education

PhD/MD/PharmD

Job description

Vir Biotechnology, Inc. seeks a Senior Vice President, Regulatory Affairs to lead the global Regulatory Affairs organization from preclinical through lifecycle management, including late-stage HDV program filings and Health Authority interactions.

The role is based in San Francisco with in-office expectations. Ideal candidate holds an advanced degree (PhD/MD/PharmD) and 15+ years of regulatory experience, with a proven track record in FDA/EMA engagements and major submissions.