Future Tech Jobs
Future Tech Jobs
This role involves leading the generation of strategic insights for a key oncology brand within GSK's ADC portfolio. Responsibilities include shaping commercial forecasts, conducting global market research, and partnering with cross-functional teams to drive business strategy and competitive intelligence.
The Director, Global Strategic Insights – Oncology role involves leading the generation of strategic insights to shape the global product strategy for a key oncology brand. Responsibilities include driving commercial forecasts, commissioning market research, and partnering with cross-functional teams to ensure insights are integrated into business decisions. The role requires a strong background in pharmaceuticals, oncology commercialization, and market research, with a focus on leveraging data to influence business strategy.
This role involves leading the development and application of AI in early phase clinical trials for AstraZeneca, focusing on Phase I/II programs. You will build and manage a team of AI researchers and engineers, develop reusable AI methods, and collaborate with domain experts to improve clinical trial design and decision-making.
This role involves leading diagnostic strategy and project execution in oncology translational medicine, supporting drug development through biomarker-driven clinical studies. The individual will oversee assay development and validation, ensure regulatory compliance, and collaborate across cross-functional teams and external partners. It emphasizes end-to-end ownership of diagnostic initiatives within a global biopharma R&D environment.
This role involves providing end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through commercial manufacturing. The Molecule Steward ensures product quality, manufacturability, and regulatory compliance by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives across the global supply chain.
The Principal Medical Writer will author and deliver high-quality clinical regulatory documents, lead cross-functional teams in developing clinical dossier documents for global regulatory submissions, and manage complex writing projects. They will interpret complex clinical and statistical information, ensuring compliance with GSK standards and regulatory requirements.
The Team Lead, Therapeutic Area Quality, leads a team of Quality Business Partners, ensuring quality is integrated into R&D programs and projects. Key responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the quality strategy and risk management.
The Team Lead, Therapeutic Area Quality, leads a team of Quality Business Partners, ensuring quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the global audit plan. The role also involves talent development and maintaining expertise in international regulations.
This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include evaluating quality strategies, driving continuous improvements, and supporting health authority inspections. The role also focuses on talent development and maintaining expertise in international regulations.
This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the quality strategy and risk management. The role requires a deep understanding of regulatory requirements and the ability to lead a global quality team.
The SERM Scientific Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. This role involves driving pharmacovigilance activities, evaluating safety data, and collaborating with cross-functional teams to ensure robust benefit-risk profiles and patient safety. The position requires significant experience in pharmacovigilance and a strong understanding of global regulations.
The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.
This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory submissions. The position requires strong technical expertise, collaboration across functions, and a focus on quality and compliance.
This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory compliance. The position requires strong technical expertise, collaboration across functions, and a focus on quality and patient safety.
This role leads translational science strategy across renal, inflammation, fibrosis, and neurodegeneration disease areas, driving biomarker development and validation to support clinical decision-making from preclinical through to launch. The position integrates cutting-edge technologies like spatial transcriptomics and human multi-omics data, working across discovery and development to de-risk clinical transitions and identify responder populations.
