Position Description Summary Acts as the operational interface for both pharmacovigilance (PV) and regulatory affairs teams, ensuring platform design, delivery, and operations support safety, compliance, and submission needs. This role will focus on optimizing platforms to streamline PV and regulatory processes, ensuring alignment with global standards and regulatory requirements. Main Responsibilities & Accountabilities Serve as point of contact for both PV and regulatory platform design, delivery, and operationsOversee the setup, integration, and ongoing governance of PV and regulatory platformsOwn and manage the PV and regulatory platform roadmap, ensuring it meets the evolving safety, regulatory, and compliance requirementsLead cross-functional collaboration with clinical, IT, and external regulatory bodies to enhance platform adoption and submission efficiencyManage platform optimization to support continuous compliance, efficiency, and scalability across both PV and regulatory domainsDrive process improvements and ensure that both PV and regulatory platforms are fully aligned with business and regulatory needsPartner with the R&D and Enterprise Data, Automation and AI teams to advance the digital capabilities to transform the R&D Operating model Qualifications & Experience Requirements Bachelor's or Masters in Life Sciences, Regulatory A...