Senior Director, Safety & Pharmacovigilance

For our client, a leader in the Pharmaceuticals & Biotech space, we are seeking a Senior Director of Safety & Pharmacovigilance. This role will drive initiatives focused on growth, customer acquisition, brand performance, and measurable demand creation within a life sciences environment. Location: San Carlos, CA (US-based candidates only; no visa sponsorship available).

About the role

You will collaborate with analytics, product, creative, and commercial teams to turn market insights into scalable campaigns, testing strategies, and performance improvements. The position offers the opportunity to directly influence customer engagement, conversion performance, and revenue growth.

Responsibilities

• Lead the development and execution of a global safety and pharmacovigilance strategy
• Oversee risk management across the product lifecycle and ensure proactive mitigation of safety risks
• Manage comprehensive safety signal detection and ensure timely resolution of safety issues
• Develop risk management plans, safety specifications, and benefit-risk assessments for regulatory submissions
• Oversee global pharmacovigilance systems ensuring compliance with international regulations
• Build and mentor a high-performing pharmacovigilance team, fostering growth and accountability
• Collaborate cross-functionally to integrate safety oversight within the organization

Qualifications

• Advanced degree (PhD, PharmD) in pharmacology or related field; MS with extensive experience also acceptable
• 10-15 years of progressive experience in pharmacovigilance or drug safety, with at least 5 years in a leadership role
• Proven expertise in global safety strategy and regulatory engagement, especially in cell/gene therapy or advanced modalities
• Strong analytical and strategic thinking skills; excellent communication and influence across the organization
• Experience with safety databases like ARGUS and ARISg; significant expertise in vaccine safety required
• Demonstrated success managing global regulatory PV submissions and health authority interactions

Pay

$285,000 – $333,000 annually

Benefits

• Hybrid work arrangement, combining remote and in-office working days
• Opportunities for professional development and career advancement
• Engagement with innovative and cutting-edge safety science initiatives
• Collaborative working environment with cross-functional teams and external partners