This role involves leading epidemiology programs, designing and delivering observational studies using real-world data, and collaborating with cross-functional teams. The position offers opportunities for growth and impact in the development and lifecycle of medical products.
This role involves leading epidemiology programs, designing and delivering observational studies using real-world data, and collaborating with cross-functional teams. The position offers opportunities for growth and impact in the development and lifecycle of pharmaceutical products.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, working with cross-functional teams to define the strategic vision and operational plan. Key responsibilities include managing the development team, ensuring regulatory approval, and aligning with GSK's oncology strategy.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, working with cross-functional teams to define the strategic vision and operational plan. Key responsibilities include managing the development team, ensuring regulatory approval, and aligning with GSK's oncology strategy.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, from early stages through approval and launch. This role involves strategic planning, team leadership, and collaboration with various stakeholders across R&D and commercial functions to ensure the successful development and commercialization of the vaccine.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, from early stages through approval and launch. This role involves strategic planning, team leadership, and collaboration with various stakeholders across R&D and commercial functions to ensure the successful development and commercialization of the vaccine.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, from early stages through approval and launch. This role involves strategic planning, team leadership, and collaboration with various stakeholders across R&D and commercial functions to ensure the successful development and commercialization of the vaccine.
The Senior Scientist role at GSK's Pilot-Plant in Ware involves manufacturing clinical trial supplies for early-phase studies, ensuring compliance with cGMP and SOPs. Responsibilities include process validation, equipment validation, and continuous improvement initiatives to enhance manufacturing efficiency and quality.
This role involves managing regulatory planning and resource management for GSK’s HIV medicines portfolio, including creating and maintaining Regulatory Development Plans, forecasting resources and costs, and supporting governance cycles. The position requires strong experience in regulatory project management, advanced knowledge of Planisware, and the ability to collaborate with cross-functional teams.
This role involves leading the operational delivery of biomarker and diagnostic strategies for GSK's oncology portfolio, particularly focusing on Antibody Drug Conjugate (ADC) development. Responsibilities include managing a team, overseeing external testing partners, and ensuring regulatory compliance and successful drug-diagnostic co-development.
This role involves leading the operational delivery of biomarker and diagnostic strategies for GSK's oncology portfolio, particularly focusing on Antibody Drug Conjugate (ADC) development. Responsibilities include managing a team, overseeing external testing partners, and ensuring regulatory compliance and successful drug-diagnostic co-development.
The Principal Programmer Analyst role involves leading statistical programming activities for clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, working in an agile, squad-based environment.
This role involves leading programming activities for clinical studies, ensuring high-quality and timely outputs. Responsibilities include mentoring junior programmers, fostering quality assurance, and collaborating with cross-functional teams to bridge scientific requirements with technical solutions.
The Principal Programmer Analyst role involves leading programming activities for clinical studies, ensuring high-quality and timely outputs. Responsibilities include mentoring junior programmers, supporting regulatory interactions, and implementing innovative solutions to improve efficiency and compliance.
This role involves leading the design and delivery of robust evidence for HIV treatment and prevention medicines. Responsibilities include shaping health economics and outcomes research strategies, collaborating with cross-functional teams, and ensuring evidence meets regulatory and payer requirements.
