Lead clinical development for vascular programs across early and late-phase trials, designing studies and translational plans to advance medicines for cardiovascular disease. Collaborate with cross-functional teams to shape clinical strategies, ensure regulatory compliance, and drive patient-focused innovation within GSK’s R&D pipeline.
Lead clinical development for vascular programmes across early and late phases, designing studies and translational plans to advance medicines for cardiovascular disease. Collaborate with cross-functional teams to shape clinical strategies, ensure patient safety, and drive innovation in drug development. Play a key role in regulatory interactions, trial oversight, and identifying transformative opportunities in vascular medicine.
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.
This role involves leading the clinical development of oncology drugs, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the company in health authority interactions. The role emphasizes data-driven decision-making and leveraging advanced analytics to enhance clinical development.
This role involves leading the clinical development of oncology drugs, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the company in health authority interactions. The position requires strong scientific and leadership skills, with a focus on leveraging data and technology to drive clinical development.
This role involves leading the clinical development of oncology treatments, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the asset in external engagements. The role emphasizes data-driven decision-making and leveraging advanced analytics.
This role involves leading the clinical development of oncology treatments, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading cross-functional teams, and engaging with health authorities and external partners. The position emphasizes leveraging advanced analytics and AI to drive decision-making and innovation in clinical development.
This role involves providing medical leadership within oncology clinical development, specifically in genitourinary (GU) cancers. The Medical Director will lead medical monitoring, ensure patient safety, contribute to study design and regulatory interactions, and interpret clinical data to inform decision-making. They will work closely with cross-functional teams and external experts to advance GSK’s oncology pipeline with a focus on high unmet need areas.
This role involves leading medical oversight and clinical strategy for genitourinary (GU) oncology trials within GSK’s R&D pipeline. The Medical Director provides physician-level expertise in study design, safety monitoring, data interpretation, and regulatory engagement, ensuring patient safety and scientific integrity. They collaborate with cross-functional teams and external experts to advance innovative cancer treatments through clinical development.
This role involves leading medical strategy and oversight for genitourinary (GU) oncology clinical trials within GSK’s R&D pipeline. The Medical Director provides physician-level expertise in study design, real-time safety monitoring, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity. They work cross-functionally within a matrix team to advance innovative cancer therapies from development through to regulatory submission and scientific dissemination.
This role involves providing medical leadership within oncology clinical development for genitourinary (GU) cancers, focusing on study design, medical monitoring, and safety oversight. The physician will interpret clinical and safety data, contribute to regulatory submissions, and engage with investigators and external experts. Working within a cross-functional team, the role ensures patient safety and clinical integrity across trials while supporting GSK’s mission to advance innovative cancer treatments.
This role involves providing medical leadership in oncology clinical development for genitourinary (GU) cancers, with responsibility for medical monitoring, safety oversight, and clinical data interpretation across trials. The Medical Director integrates physician expertise into study design, regulatory interactions, and cross-functional decision-making, working within a global matrix team. The position requires deep oncology knowledge, experience in clinical trial conduct, and strong collaboration with internal teams and external experts.
This role involves providing medical leadership in oncology clinical development, specifically for genitourinary (GU) cancers. The Medical Director will lead medical monitoring, contribute to protocol design, interpret clinical data, and ensure patient safety across clinical trials. They will work closely with cross-functional teams, engage with external experts, and support regulatory submissions and scientific communications within a global pharmaceutical environment.
Lead scientific strategy for oncology clinical studies, contributing to protocol design, data interpretation, and regulatory deliverables within a global pharmaceutical environment. Collaborate across functions to ensure scientific rigor and alignment with clinical development goals, while engaging with external experts and supporting regulatory submissions. The role emphasizes innovation, data-driven decision-making, and continuous improvement in clinical development processes.
Provides scientific leadership in oncology clinical development, contributing to study design, data interpretation, and regulatory documentation within a defined clinical programme. Works closely with cross-functional teams to ensure scientific rigor and alignment with clinical strategy, while supporting the execution of clinical studies from early to late stages. Focuses on generating robust clinical insights to advance cancer therapies with high unmet need.
