Associate Director/Senior Manager, PV

Associate Director/Senior Manager, PV (Pharmacovigilance) Operations Location: UK London, New Oxford Street Posted Date: Dec 12 2025 The key purpose of this role is to support Pharmacovigilance Operations "PV Ops" ICSR Management in activities such as ICSR management, clinical trial/program interactions, Argus configuration for submissions to regulatory authorities, partners, and CROs. We provide a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. Hybrid working model available through Performance with Choice programme. Responsibilities Supervise a team of up to 10 scientific staff (global/local) supporting ICSR management activities. Manage the team to ensure appropriate prioritisation and time management in line with business needs. Build external relationships with key stakeholders and senior leaders. Provide project management and case processing oversight for clinical trials and post‑marketing programs, supporting spontaneous case processing activities and ensuring timely completion of deliverables. Provide support and guidance to ICSR management leads and team members to ensure compliance with global regulations and adherence to GSK SOPs. Resolve issues and concerns within the ICSR management team and, where resolution is not possible or impacts PV Ops, raise them to the ICSR management director. Ensure all ICSI management activities are appropriately resourced and raise any resourcing issues. Provide workload forecasts and work with the ICSR management director to strategically plan in line with business goals. Develop the team, identify training requirements and work with the training team to establish a training plan. Provide strategic advice to the function and oversee direct or indirect reports performing PV activities. Mentor new staff during onboarding. Use influencing skills to drive best practice and innovation across PV Ops. Enhance matrix management across PV Ops, ensuring successful connections with PV Ops sub‑teams. Basic Qualifications & Skills Degree in life sciences or related field, or equivalent experience. End‑to‑end case processing knowledge from intake to submission and experience managing teams performing these processes. In‑depth knowledge of pharmacovigilance concepts and project management within PV, including regulatory requirements, documentation, process design, implementation, and writing standards. Experience in clinical trials from a PV perspective (or post‑marketing PV); candidates with either may be considered for a suitable team fit. Functional oversight and team management experience, ideally at associate director or manager level. Preferred Qualifications & Skills Experience with inspections and audits in PV. Technological experience, such as working on automation or AI projects, rolling out new technology, or serving as an SME. Ability and willingness to adapt to new technology and automation trends in PV. Closing Date for Applications 28th of December, 2025 (COB) Equal Opportunity Statement GSK is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex (including pregnancy, gender identity and sexual orientation), parental status, national origin, age, disability, genetic information, military service or any basis prohibited under federal, state or local law. Adjustments Should you require adjustments to our process to demonstrate your strengths, contact UKRecruitment.Adjustments@gsk.com. If your enquiry does not relate to adjustments, we will not be able to support you through these channels. #J-18808-Ljbffr