Jobs at GSK

Lead CMC regulatory strategy for development and lifecycle activities. Coordinate and author CMC submission content, manage complex projects and inspections support, advise on global regulatory requirements, mitigate submission risks, and influence regulatory decisions across cross-functional teams to ensure timely product access and uninterrupted supply.

Lead strategic, multi-stakeholder oncology account engagement across New England and Upstate New York to drive formulary and on-label access. Develop account plans, present clinical and economic value propositions, negotiate contracts, coordinate cross-functional teams, forecast performance, maintain CRM, and represent GSK at industry events to advance product adoption and access.

Lead and coach a regional team of Strategic Oncology Account Directors to execute account-based strategies across health systems, cancer centers, and community oncology networks. Align brand, access, and account plans with cross-functional partners to drive access, formulary inclusion, contracts, and market growth. Oversee account planning, KPI-driven performance reviews, negotiation support, and compliant external engagement while representing GSK at industry events.

As an Electrical Engineer at GSK, you will manage electrical services, ensure compliance with standards, and improve electrical systems to enhance operational safety and efficiency.

Lead CMC regulatory strategy and execution for mature vaccine projects, manage global CMC regulatory activities across development, registration, and lifecycle management, prepare and review regulatory submissions (e.g., eCTD Module 3), serve as FDA liaison, advise cross-functional teams on GMP and regulatory requirements, identify risks and mitigation strategies, and mentor team members.

The Account Manager is responsible for managing B2B relationships in complex healthcare networks, achieving sales targets, and delivering clinical presentations. The role involves analyzing market trends and collaborating with internal teams to enhance customer engagement.

Lead a translational genetics team to apply statistical genetics and integrate genetics, genomics (including proteomics) and clinical data to inform target validation, biomarker discovery, indication and subgroup selection. Provide strategic leadership, hands-on analytical expertise, cross-functional project support, external collaborations, and communicate findings to senior stakeholders to accelerate drug discovery and development.

Lead safety evaluation and risk management for oncology assets across clinical development. Drive signal detection, integrated safety analyses, regulatory safety inputs, and cross-functional mitigation strategies. Represent SERM on project teams, present risks to governance, partner with safety physicians and regulators, and mentor junior staff to ensure timely, high-quality safety decisions.

Own B2B relationships with large health systems and key stakeholders to drive formulary adoption and product utilization. Develop and execute territory and key-account plans, deliver clinical brand presentations, meet sales targets, and collaborate with cross-functional teams while adhering to compliance and company policies. Travel up to 50% to cover assigned territory.

The Senior Director will lead biologics manufacturing innovations, drive technology transfers, and manage a global team while enhancing product performance and complying with regulations.

Develop scalable cloud infrastructure and robust software solutions for AI/ML, collaborating with engineers and scientists to enhance scientific research.