Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...
This role involves managing technology transfer projects for external contract manufacturing organizations (CMOs) in the pharmaceutical sector, ensuring alignment between GSK and suppliers on timelines, quality, and technical deliverables. The specialist will coordinate cross-functionally across procurement, quality, technical, and supply teams to operationalize new assets or suppliers, with a focus on sterile drug products like monoclonal antibodies and vaccines. Key responsibilities include maintaining critical path schedules, mitigating risks, and driving project governance from transfer through to product launch.
This role involves managing technology transfer projects for external contract manufacturing organizations in the pharmaceutical sector, ensuring alignment between GSK and suppliers. The specialist will oversee project schedules, mitigate risks, and ensure timely delivery of drug products across critical assets like monoclonal antibodies, vaccines, and small molecules. Collaboration with cross-functional teams and supplier relationship management are central to driving successful operationalization within budget and timeline.
This role involves leading the development and implementation of AI and digital health strategies to transform clinical development processes. The Senior Strategy Director will act as a trusted advisor, designing digital solutions for patient recruitment, remote monitoring, and data collection while driving innovation through AI. They will lead cross-functional teams, shape operating models, and ensure digital tools are integrated into clinical protocols with a focus on measurable value and patient outcomes.
This role involves shaping AI and digital health strategies to accelerate clinical development within a collaborative, innovation-driven team. You'll work across project design, protocol development, and digital solution implementation, supporting pharmaceutical partners and AstraZeneca R&D. The position emphasizes strategic consulting, technical evaluation of digital tools, and driving value through scalable, patient-centric innovations in clinical trials.
This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.
The Laboratory Technician will support the Immunoassay group by executing experimental work, maintaining the lab, and ensuring high-quality data for clinical trials. The role involves hands-on lab work, preparing reagents, conducting assays, and maintaining compliance with safety and regulatory guidelines.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMOs, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.
This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across EMEA and other highly regulated markets. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of identified risks and corrective actions.
This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, forming strategic partnerships, and ensuring clinical relevance in all analytical platforms.
This senior role involves leading and maintaining a robust pharmacovigilance quality assurance programme, ensuring compliance with global regulations and internal standards. Key responsibilities include overseeing PV processes, managing audits, and providing strategic guidance to ensure patient safety and continuous improvement.
This role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the GSK Global Supply Chain. You will evaluate compliance with regulatory requirements and provide sterile manufacturing expertise, engaging with senior stakeholders and producing clear audit reports.
