Leads clinical development for respiratory assets, designing and executing clinical and translational strategies to advance drug candidates. Provides medical oversight, contributes to regulatory submissions, and collaborates across functions to deliver innovative medicines. Focuses on patient-centric innovation and scientific rigor in a matrix environment.
This role involves leading clinical development for respiratory assets within GSK’s Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and deliver clinical and translational strategies, oversee study execution, ensure patient safety, and contribute to regulatory submissions. Working cross-functionally, they will help shape development plans that align with scientific innovation and patient needs, particularly in pulmonary hypertension and related areas.
This role involves collaborating with scientists and engineers to build robust, reproducible data pipelines for diverse research projects. You will ensure datasets are accurate, version-controlled, and ready for machine learning, working hands-on with cutting-edge technologies and methodologies.
Design and operate secure, scalable Oracle Cloud Infrastructure (OCI) platforms supporting enterprise applications, scientific research, and AI workloads. Implement Infrastructure as Code with Terraform and CI/CD, enforce cloud security controls, and provide self-service cloud patterns for research and engineering teams. Focus on automation, monitoring, disaster recovery, and cost optimisation across cloud services.
The Data-Flow Lead role at GSK involves designing and governing data-flows for the R&D division, ensuring data is trusted, reusable, and compliant. Responsibilities include translating business needs into technical requirements, developing modular data-flows, and integrating diverse data sources into a unified format.
The Data-Flow Specialist role at GSK involves designing, developing, and maintaining modular end-to-end data flows for the R&D division. Key responsibilities include ensuring compliance-by-design, integrating diverse data sources, and coaching the team on best practices.
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 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 Data-Flow Specialist role at GSK involves designing, developing, and maintaining modular end-to-end data flows for the R&D division. Responsibilities include ensuring compliance-by-design, integrating diverse data sources, and coaching the team on best practices.
The Data-Flow Specialist role at GSK involves designing, developing, and maintaining modular end-to-end data flows for the R&D division. Responsibilities include integrating diverse data sources, ensuring compliance, and coaching the team on best practices.
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 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 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 of new medicines.
This role involves leading epidemiology programs, designing and delivering observational studies using real-world data, and providing scientific advice to asset teams. The position requires a master’s degree in a quantitative field and at least 5 years of applied epidemiology experience.
