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Tier-1 employer and metro location increase competition, but niche pharmacovigilance specialization limits applicants.
Deep pharmacovigilance and regulatory expertise required makes skills less transferable across industries.
Explicit 8–14 years and mandatory pharmacovigilance, GxP, CSV, and platform experience create strict filters.
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Own end-to-end technology management of Safety and Medical platforms including strategy, delivery, operational performance, and compliance.
Lead backlog prioritization and Agile delivery for enhancements and new capabilities supporting pharmacovigilance, medical affairs, regulatory compliance, and related functions.
Manage vendor relationships, service levels, and ensure continuous improvement and adoption of technology solutions in Safety and Medical domains.
8 to 14 years of relevant experience in Pharmacovigilance, Drug/Product Safety, Medical Affairs or Medical Information technology.
Expertise with one or more Safety and Medical platforms such as Veeva Safety, ArisGlobal LifeSphere, Oracle Argus Safety, or similar.
Strong knowledge of Pharmacovigilance regulations, GxP compliance, Computer System Validation, and Global Health Authority requirements.
Experience with Agile product delivery and managing SaaS or enterprise technology products.
Experienced in delivering technology solutions within Safety and Medical domains, balancing innovation and regulatory compliance.
Strong stakeholder management skills across Safety, Medical, Clinical, Regulatory, and Quality functions, working in cross-functional global teams.
Capable of driving technology roadmaps, leveraging AI/automation, and managing complex vendor ecosystems to optimize operational and compliance outcomes.