This role involves leading the development and application of quantitative systems pharmacology models to enhance drug discovery and development. Responsibilities include building mechanistic models, collaborating with cross-functional teams, and driving model-informed drug development strategies.
This role involves leading the development and application of quantitative systems pharmacology (QSP) models to advance drug discovery and development. Responsibilities include building mechanistic models, collaborating with cross-functional teams, and driving model-informed drug development strategies.
Leads the design and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across the product lifecycle. Translates customer and payer needs into robust scientific evidence, collaborating with cross-functional teams to inform market access, reimbursement, and value-based pricing strategies. Focuses on generating high-quality, decision-ready data using diverse real-world data sources and advanced study methodologies.
Leads the design and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across their lifecycle. Focuses on generating robust, scientifically credible data to inform value propositions, market access, and reimbursement strategies. Collaborates with cross-functional teams and external experts to align evidence generation with payer, clinician, and regulatory requirements.
This role involves leading the development and deployment of Lab-in-an-Automated-Loop (LIAL) systems, integrating computational intelligence with physical laboratory experimentation. Responsibilities include collaborating with cross-functional teams to design and implement integrated systems, driving innovation with AI and data automation, and mentoring early-career scientists.
This role involves developing and executing global and regional regulatory strategies for oncology assets, ensuring optimal labelling and approvals while maintaining compliance. You will collaborate with cross-functional teams to shape development plans and regulatory interactions across multiple regions, with a focus on clear thinking, collaboration, and a patient-first mindset.
This role involves leading clinical development activities for GSK’s oncology portfolio, with a focus on genitourinary (GU) cancers. The Senior Medical Director will design and execute Phase 1-3 clinical trials, provide medical oversight, interpret clinical data, and engage with external experts and regulatory authorities. The position requires strong leadership in a matrixed environment and deep expertise in oncology drug development.
The Associate Director, Pipeline Project Management for Business Development at GSK manages R&D projects from early diligence through integration and transition to business as usual. Key responsibilities include cross-functional planning, risk management, and ensuring smooth knowledge transfer and execution of BD transactions.
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.
The Associate Director (Scientific Data and Publications) manages GSK's external scientific content and data licenses, ensuring cost-effective and compliant access to critical information. The role involves strategic portfolio management, vendor relationships, and leveraging AI for future needs.
The Automation Engineer role at GSK involves providing technical expertise for automation and control systems in a pharmaceutical manufacturing environment. Responsibilities include supporting new and existing equipment, ensuring compliance with standards, and collaborating on continuous improvement initiatives.
This role involves leading the design and execution of experiments for antibody and protein discovery, using yeast-based and phage display platforms, in silico design tools, and other innovative technologies. The scientist will work in a lab-centric environment, contributing to the development of therapeutic antibodies and proteins, and collaborating with matrix teams on various disease targets.
This role involves working in a lab-centric environment, focusing on antibody discovery and engineering using yeast-based and phage display platforms, combined with in silico design tools. The position offers opportunities to develop skills in molecular biology, AI-driven protein design, and collaboration within a dynamic team of experts.
This role involves practical laboratory work in R&D, focusing on the development and deployment of advanced processes and technologies for pharmaceutical manufacturing. You will work closely with chemists and material scientists to build process understanding, optimize scale-up, and ensure successful commercialization of GSK medicines.
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.
