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The Principal Scientist will lead the externalization team for drug substance development, managing CRO collaborations and ensuring project deliverables meet quality and regulatory standards.

The Senior Manager will oversee third-party quality strategies for compliance with GMP standards, ensuring quality oversight and driving process improvement across external providers for GSK R&D.

The Director oversees real-world data projects, providing biostatistical expertise, managing staff, and ensuring regulatory compliance while fostering innovation in analytics.

The CRM Tech Lead will implement CRM strategies for Japan, utilize Veeva CRM, enhance Omnichannel marketing, and manage CRM projects while ensuring compliance with GSK standards.

As a QC Senior Analyst, you'll validate methods, support inexperienced staff, introduce new lab equipment, and respond to regulatory queries.

The AI Software Engineer focuses on creating AI solutions for digital twins, enhancing supply chains and manufacturing. You will ensure compliance, collaborate on product development, and lead AI initiatives for better patient outcomes.

As a Biostatistician Trainee, you'll assist in statistical analyses, collaborate with teams, ensure compliance with guidelines, and participate in data discussions.