Franklin, MA – Prestige is excited to announce the successfully completed search for an Associate Director of Pharmacovigilance Operations Contractor for a clinical-stage biotechnology partner.
The individual hired for this role brings deep pharmacovigilance and drug safety operations expertise, with significant experience supporting clinical and post-marketing safety activities within fast-paced biotech environments. They have led case processing oversight, vendor management, safety database operations, and cross-functional safety governance, ensuring compliance with global regulatory requirements and inspection readiness.
In this critical role, they will oversee day-to-day pharmacovigilance operations, including ICSR processing, aggregate report support, safety system oversight, and vendor performance management. They will partner closely with Clinical Development, Regulatory, Quality, and external CRO partners to ensure timely, high-quality safety deliverables. Leveraging strong operational rigor and a proactive, solutions-oriented mindset, they will strengthen PV infrastructure, enhance processes, and help scale safety operations to support the company’s advancing clinical pipeline.
Congratulations to our Drug Safety search team for this successful project!
About Prestige Scientific:
Prestige Scientific is an executive search firm that advises our clients on recruiting impactful leaders. We provide our clients with a performance-based hiring system that identifies leaders with past success meeting similar corporate objectives as their own, while overcoming challenges and adhering to critical timelines. We have dedicated experts in eleven practice areas that mirror a typical biopharma company, allowing us to support our client's growth from Discovery through Commercial.
