Lead clinical development for vascular programmes across early and late-phase studies, shaping clinical plans and study designs to accelerate safe, meaningful medicines for vascular disease. Work cross-functionally with translational science, regulatory, safety, and commercial teams to deliver clinical development strategies and drive innovation in cardiovascular medicine.
Lead clinical development for cardiovascular assets within GSK's Respiratory, Immunology & Inflammation Research Unit, driving translational and clinical strategies from early to late stages. Provide medical oversight, design studies, and collaborate across functions to deliver innovative medicines addressing unmet patient needs. Work in a hybrid model with a future relocation to Cambridge.
This role involves planning, designing, and executing multiple studies to support the launch and market positioning of GSK's oncology medicines. The Director will collaborate with internal and external stakeholders to generate robust real-world evidence and cost-effectiveness analyses, ensuring strategic alignment and effective communication.
Leads the design and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across the product lifecycle. Collaborates with cross-functional teams to generate robust data for regulatory, reimbursement, and market access decisions. Engages with internal stakeholders and external experts to align scientific research with payer and clinician needs, ensuring evidence impacts patient access and commercial success.
This role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include leading the prioritization of AI opportunities, building and testing prototypes, and shaping deployment strategies with cross-functional teams.
This role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include leading AI opportunity prioritization, building and testing prototypes, and shaping build-buy-partner decisions.
This role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include leading the prioritization of AI opportunities, building and testing prototypes, and shaping deployment strategies with cross-functional teams.
This role involves driving the AI-native Development Operations strategy at GSK, identifying and prototyping AI opportunities, and leading the deployment of AI-enabled workflows. The Director will work with business SMEs, technology teams, and external partners to ensure scalable and compliant solutions.
This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, contributes to regulatory engagements, and mentors medical teams within a cross-functional environment. The position integrates physician expertise into clinical strategy and external scientific forums, focusing on advancing care in high unmet need cancers.
This role involves leading clinical development in oncology, with a focus on lung cancer, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and mentor junior medical staff within a global matrix team. The position emphasizes strategic input, external scientific engagement, and integration of clinical insights to advance therapies for high unmet need.
This role involves leading clinical development for oncology, specifically in lung cancer, by providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and mentor junior medical staff. The position requires deep expertise in oncology clinical trials and close collaboration with cross-functional teams and external experts.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, protocol development, and collaboration with cross-functional teams and external experts.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. This role involves leading medical monitoring, ensuring patient safety, and collaborating with cross-functional teams to integrate medical considerations into study execution and regulatory interactions.
The Medical Director, Oncology Clinical Development role involves leading medical monitoring, safety oversight, and clinical data interpretation for clinical studies in lung and head/neck cancers. The role requires strong clinical expertise, collaboration with cross-functional teams, and engagement with external experts to ensure patient safety and study integrity.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, and collaboration with cross-functional teams to ensure patient safety and clinical integrity.
