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.
The Medical Director, Oncology Clinical Development will lead clinical research activities, develop and execute oncology clinical trials, and engage with key external experts. Responsibilities include protocol development, medical monitoring, safety data review, and collaborating with various stakeholders to advance GSK’s clinical portfolio.
The Medical Director, Oncology Clinical Development, will lead clinical research activities to advance GSK’s oncology portfolio. Key responsibilities include developing and executing phase 1-3 clinical trials, collaborating with cross-functional teams, and engaging with key external experts to ensure the successful development and regulatory approval of innovative oncology treatments.
The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing the development of antibody drug conjugates (ADCs) for solid tumors. Key responsibilities include collaborating with multidisciplinary teams to design and execute clinical trials, ensuring high-quality protocol development, and engaging with key external experts to drive data generation and regulatory approvals.
The Medical Director, Oncology Clinical Development, will lead the clinical research activities for GSK’s oncology portfolio, including developing and executing phase 1-3 clinical trials. They will collaborate with various stakeholders to ensure high-quality protocol development, medical monitoring, and data interpretation, while also engaging with key external experts and thought leaders.
As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.
This role involves leading the scientific design and execution of interventional clinical studies in oncology or hematology, ensuring high standards of quality and ethics. You will collaborate with cross-functional teams, provide scientific oversight, and engage with healthcare professionals to deliver impactful results.
The Quality Validation and CSV Manager will lead a team responsible for ensuring all validation activities, including process, cleaning, facility, and computer systems validation, comply with regulatory requirements and GSK quality standards. The role involves managing validation protocols, collaborating with cross-functional teams, and providing technical expertise and training.
This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategies. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.
This role involves leading a global matrix programme team to transform incoming material testing and data management across GSK's manufacturing sites. Responsibilities include defining future-state operating models, creating global standards, and ensuring harmonised QC master data structures while partnering with various teams to implement the strategy.
This role involves leading a global matrix programme team to transform incoming material testing and data management across GSK's manufacturing sites. Responsibilities include defining future-state operating models, creating global standards, and ensuring harmonised QC master data structures while partnering with various teams to implement the strategy.
This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive strategic alliances and complex collaborations.
This role involves leading Extractables and Leachables (E&L) assessments for biopharmaceutical manufacturing processes, container closure systems, and dosing devices. The Specialist will work with internal and external labs to ensure E&L testing is completed scientifically, compliantly, and cost-effectively, while also managing risk identification and escalation.
This role involves leading the development and deployment of advanced in-silico protein engineering and design principles to generate complex reagents for drug discovery. You will collaborate with computational experts, protein expression teams, and external partners to design, generate, and test engineered proteins, contributing to scientific innovation and project delivery.
