Vice President, Pharmacovigilance

Responsibilities

• Develop and implement pharmacovigilance processes, policies, SOPs, and safety database/PV systems.
• Lead cross-functional governance, benefit-risk assessment, signal detection, and risk management efforts.
• Chair the executive safety review committee, oversee safety data exchange with partners, and contribute to industry-wide safety initiatives.
• Partner with clinical development to integrate safety into protocols, risk management plans, and safety charters.
• Provide PV oversight for regulatory filings (IND/BLA/MAA) - including Clinical Overviews, ISS, and RMPs - and review IBs, DSURs, and key CSR sections; participate in regulatory meetings as needed.
• Lead medical review of ICSRs and oversee PV team operations, quality, and compliance with global safety regulations.
• Monitor and assess CRO performance on pharmacovigilance activities.

Qualifications & Education

• MD, with clinical and industry experience and a proven track record leading pharmacovigilance teams.
• Minimum of 15 years' experience in drug safety and pharmacovigivalnce roles in the biotech or pharmaceutical industry.
• Proven leadership expertise, including a track record of building and leading high-performing teams.
• In-depth knowledge of global pharmacovigilance regulations and compliance requirements (EMA/FDA/ICH).
• Strong leadership and strategic decision-making abilities to drive safety initiatives and ensure regulatory compliance.

Benefits

• Immunic Therapeutics is an Equal Opportunity Employer.
• We are committed to fostering a diverse, inclusive, and equitable workplace where all individuals are valued and respected.
• Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, sexual orientation, national origin, disability, veteran status, or any other protected status.

Pay

$330K - $410K