This role involves leading the generation and dissemination of real-world evidence and health outcomes research for RSV vaccines. Responsibilities include managing data generation plans, collaborating with cross-functional teams, and engaging with external stakeholders to ensure robust evidence supports vaccine development and commercial success.
This role involves leading the generation and dissemination of real-world evidence and health outcomes research for GSK's RSV vaccines. Responsibilities include managing data generation plans, collaborating with cross-functional teams, and engaging with external stakeholders to ensure robust evidence supports product positioning and market access.
This role involves leading the development of digital products for content generation and collaboration in GSK's R&D department. Responsibilities include creating product vision, managing technical dependencies, and driving AI-first solutions to improve content authoring processes.
This role involves leading a team responsible for risk and compliance in GSK's R&D technology areas, providing hands-on consulting and assurance, and managing relationships with stakeholders. The position requires a deep understanding of cyber security, risk management, and compliance in a regulated environment.
This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials, contributing to study design, data interpretation, and regulatory interactions. The Medical Director integrates physician-level expertise into clinical development, working within cross-functional teams to ensure patient safety and scientific integrity. The position plays a key role in translating clinical data into actionable insights for advancing cancer treatments with high unmet need.
This role involves leading medical oversight in gastrointestinal (GI) oncology clinical development, ensuring patient safety and clinical integrity across study design, execution, and data interpretation. The Medical Director collaborates with cross-functional teams to integrate physician insights into clinical trials, engages with external experts and regulators, and contributes to regulatory submissions and scientific communications. The position requires deep expertise in oncology and clinical development within a global pharmaceutical environment.
This role involves serving as the physician lead within an oncology clinical development team, providing medical expertise in study design, safety oversight, and data interpretation for gastrointestinal (GI) cancer trials. The Medical Director ensures patient safety and clinical integrity across clinical studies, collaborates with cross-functional teams and external experts, and contributes to regulatory submissions and scientific communications. The position supports GSK’s mission to advance innovative cancer treatments grounded in disease biology and real-world impact.
This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials within GSK’s global development programme. The Medical Director provides physician-level expertise in study design, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity across phases I–III. Working within a cross-functional matrix team, the role integrates medical insight into clinical strategy and collaborates with external experts and investigators to advance innovative cancer therapies.
The Medical Director, Oncology Clinical Development - GI, provides medical expertise and oversight for clinical studies, ensuring patient safety and clinical integrity. The role involves leading medical monitoring, interpreting clinical data, and collaborating with cross-functional teams to advance oncology treatments.
Leads clinical operations strategy and execution across the full lifecycle of a key asset, ensuring operational feasibility, regulatory compliance, and high-quality delivery of clinical studies. Works cross-functionally to align study design with scientific vision, manages vendor and resourcing strategies, and drives innovation in patient-centric trial execution. Serves as primary point of accountability for global clinical operations at the asset level.
Leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to align study execution with scientific and regulatory goals, driving innovation and efficiency while managing risk and stakeholder engagement. Focuses on patient-centric approaches and inspection readiness within a global, matrixed environment.
Leads clinical operations for a key asset across its full lifecycle, ensuring operational strategy aligns with scientific goals and regulatory requirements. Oversees study delivery, vendor and resourcing strategy, risk management, and cross-functional coordination. Ensures inspection readiness and high-quality data output while leading matrixed teams and influencing senior stakeholders globally.
Leads clinical operations strategy across the full asset lifecycle, ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to shape clinical development plans, manage vendor and resourcing strategies, and maintain inspection readiness. Focuses on patient-centric, efficient study execution within a global, matrixed environment.
Leads clinical operations strategy and execution across the full lifecycle of a drug development asset, ensuring high-quality, compliant, and efficient delivery of global clinical trials. Works cross-functionally to shape development plans, manage risk, and align operational delivery with scientific and regulatory goals. Provides strategic leadership to study teams and represents clinical operations at senior governance levels.
Leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to align study execution with scientific and regulatory goals, driving innovation and efficiency while managing risks and stakeholder engagement. Serves as the primary accountability point for clinical operations within global governance structures.
