# Senior Manager, Regulatory Asset Oversight at GSK

GSK is hiring a Senior Manager, Regulatory Asset Oversight. Level rates it Little AI ●○○○; you can [apply on GSK](https://jobsbylevel.com/go/cc958a1b-79c0-4eb1-b733-75aa12af977f?utm_medium=ai-agent).

AI Level 1, AI centrality 37 out of 100. Remote (Mississauga Milverton Drive).

## Details

- Company: [GSK](https://jobsbylevel.com/companies/gsk)
- AI level: AI Level 1 (score 37 out of 100)
- Location: Remote (Mississauga Milverton Drive)
- Posted: November 12, 2026
- Apply: https://jobsbylevel.com/go/cc958a1b-79c0-4eb1-b733-75aa12af977f?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=senior-manager-regulatory-asset-oversight-at-gsk-526336

## Description

Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together. Find out more: Our approach to R&D Position Summary The Senior Manager, Regulatory Asset Oversight will partner with the GRL (Global Regulatory Lead) and Regulatory Matrix Teams (RMT) and Early/Medicine Development Teams to provide over-arching project management support to active Rx and Vx projects across the lifecycle of the asset. As Senior Manager, Regulatory Asset Oversight you will create and manage integrated regulatory plans, and ensure team is on track to deliver per the Regulatory strategy. Will be responsible for ensuring a consistent approach to Regulatory Asset oversight activities within and across project teams which best serve R&D Pipeline and key Established Products goals and ultimately the Patient. Collaborates and networks across the R&D matrix to ensure that project management and submission oversight activities are agreed and aligned to efficiently support R&D portfolio aspirations. Coordinates with Submission Delivery Excellence colleagues on the operational execution of the strategy. This role requires leadership within and across enterprise matrix teams including GRA (both central and at the Local Operating Company level), GRO, and contributing departments (e.g. Clinical Operations, Data Management, Stats and Programming) as needed to facilitate submission delivery expectations. We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Develop and maintain a holistic view of the global regulatory integrated plan at the asset level in collaboration with the GRL and RMT. Drive the execution of agreed plans, performing scenario planning, impact analyses, and risk mitigation. Assist RMTs and GRLs with submission delivery strategies that align with R&D objectives, e.g. Hyper-Acceleration, Acceleration in regions Implement a structured approach with assigned RMTs to ensure that the submission delivery strategy is aligned with the Global Submission Strategy (GSS) throughout the late-stage Development lifecycle Proactively partner as a Single Point of Contact with RMT, Submission Coordination, and Publishing colleagues to ide Promote and drive the use of integrated Regulatory technologies to provide real-time, accurate submission status information (visuals and reports) for RMTs to highlight compliance from central dispatches through to registrations across markets. Maintains meaningful metrics and KPIs to assess individual and team performance which are aligned across the Regulatory Asset Oversight function. Why You? Basic Qualifications We are seeking professionals with the following required skills and qualifications to help us achieve our goals: Degree in a biological, healthcare, or scientific discipline or extensive experience within the drug development environment. 5 years of regulatory affairs experience or similar

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/senior-manager-regulatory-asset-oversight-at-gsk-526336

Source: https://jobsbylevel.com/jobs/senior-manager-regulatory-asset-oversight-at-gsk-526336

## Cite this page

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