Vice President, Pharmacovigilance & Risk Management
Celldex
September 03, 2026
Full-time
Remote friendly (Hampton, NJ)
Worldwide
Operations
Role: Vice President of Pharmacovigilance & Risk Management, overseeing global safety strategy and operations from clinical development through commercialization. Responsibilities: lead pharmacovigilance infrastructure, ensure compliance with global regulations, manage safety surveillance activities (ICSRs, signal detection, benefit-risk assessments), develop risk mitigation plans, support regulatory submissions, and lead cross-functional safety collaborations. Requirements: MD with extensive experience (>15 years) in pharma/biotech drug safety, deep expertise in global pharmacovigilance regulations, proven leadership in late-stage development and product launches, and strong stakeholder management skills. Preferred: experience in immunology, allergy, dermatology, or related therapeutic areas; experience scaling pharmacovigilance systems in biotech environments; familiarity with safety systems implementation. HighValue: immunology/autoimmune therapeutic focus, late-stage development, global regulatory compliance, drug safety leadership, and cross-functional collaboration. WorkSetup: not specified, but role involves strategic leadership across clinical and commercial phases.