Support the President, Europe by managing complex calendars, travel, communications, and large-scale events, while overseeing stakeholder interactions and administrative processes.

The SERM Scientific Director leads pharmacovigilance and risk management for GSK assets, ensuring safety evaluation, regulatory submissions, and cross-functional team collaboration in clinical and post-marketing settings.

The Head of RII or Oncology Programming is responsible for overseeing clinical data transformation into regulatory-ready evidence, leading a global programming organization, ensuring delivery excellence, and championing innovation in clinical programming.

Lead global CMC regulatory strategy for biological products, collaborating across R&D, supply, and quality teams to ensure compliance and approval of applications. Oversee regulatory submissions and risk mitigation efforts while mentoring colleagues and identifying process improvements.

Lead global sterility assurance strategy across manufacturing, ensuring compliance, improving capability, and implementing standards while overseeing inspection readiness and risk controls.

The Document & Information Lead manages document control processes for major projects, ensuring compliance and data integrity while leading the document team and handling stakeholder communication.

Provide high-quality executive support to senior leaders by managing complex calendars, travel arrangements, and stakeholder communications while leading process improvements.

The Executive Assistant will support the GSK Oncology GPS SVP, managing calendars, travel, meetings, and correspondence, while ensuring compliance with policies.

Manage capital projects in R&D, from inception through delivery, ensuring adherence to compliance, quality, and safety. Collaborate with stakeholders on scope, budget, and timelines while leading multidisciplinary teams.

Lead statistical activities in oncology studies, employing innovative statistical methods to guide development decisions and ensure regulatory compliance.

The Statistics Graduate Programme offers hands-on experience through rotations, focusing on statistical analysis and evidence generation across various medical disciplines, including biostatistics, oncology, and real-world data.

The role involves developing regulatory policy and advocacy strategies, collaborating with teams, analyzing regulatory information, and building relationships with stakeholders to advance GSK's policy objectives.