1 of 1 Permanent Document Management Jobs in Maidenhead

Main Responsibilities & Accountabilities Serve as point of contact for both PV and regulatory platform design, delivery, and operations Manage platform implementations, updates, and optimization of system solutions for regulatory document management, registration tracking, compliance management, submission, publishing, and safety case processing Oversee the setup, integration, and ongoing governance of PV and regulatory platforms Own and manage the … PV and regulatory platform roadmap, ensuring it meets the evolving safety, regulatory, and compliance requirements. Responsible for lifecycle management, governance, release planning, and operational health for these platforms Build and maintain strong relationships with regulatory and PV business stakeholders, ensuring their requirements are captured and prioritized in platform design and process optimization. Lead cross-functional collaboration with clinical, IT … Experience Requirements Bachelor's or Masters in Life Sciences, Regulatory Affairs, Health Informatics, or related field 12+ years of experience in pharmacovigilance, regulatory affairs, R&D operations, or platform management Expertise in safety data systems, regulatory submission processes, and platform technologies (e.g., Veeva Regulatory and Safety, Argus Safety Solutionsetc.) Proven leadership in managing cross-functional teams, projects, and vendor More ❯