Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
This position will lead the transformation of project leadership capabilities across the R&D enterprise. On a systemic level, this role will prepare critical GPL roles (Exec Directors) to be CEO of the project via a bespoke leadership/drug development/executive training and...
This role involves leading the strategic sourcing and evaluation of external innovation opportunities in Hematology and Cardiovascular/Renal therapeutic areas. Responsibilities include identifying high-potential assets, shaping early partnering strategies, and driving transactions in collaboration with Business Development.
At GSK, we unite science, technology and talent to get ahead of disease together. We are looking for an experienced and strategicHR Business Partner to join our Global Human Resources team, supporting ourDevelopment Operations organisation.This is an exciting opportunity to...
Develops and executes internal communications strategies to support organizational change and strategic priorities at a global biopharma company. Works closely with senior leaders to craft messaging, drive employee engagement, and manage change through compelling content and data-driven insights. Focuses on building confidence during transformation using storytelling, AI, and cross-functional collaboration.
Regulatory Affairs ManagerType: PermanentLocation: Pancras Square, LondonIntroduction to roleDeliver and maintain competitive licences for the UK, driving regulatory strategy for new initiatives and ensuring regulatory compliance for defined product and project responsibilities, including project leadership. Achieve timely delivery of clinical...
The Senior Statistician I will lead statistical input into clinical and preclinical study design, analysis, and reporting within AstraZeneca’s CVRM team. This role involves developing robust statistical analysis plans, applying modelling and simulation techniques, and translating complex results into actionable insights for multidisciplinary teams. The position emphasizes methodological rigor, regulatory readiness, and collaboration across global therapy areas to accelerate evidence generation for innovative medicines.
This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA activities, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.
This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading regulatory discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.
The Global Study Lead is responsible for managing the full lifecycle of clinical studies, from design and planning to execution and documentation. Key responsibilities include leading the study team, ensuring compliance with regulations, managing budgets, and collaborating with cross-functional teams and external partners to deliver high-quality study results.
The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharm, vaccines, and pharmaceutical facilities. Responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports. The role requires strong communication skills and subject matter expertise in sterile manufacturing.
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, collaborate with R&D and clinical development, and establish high-value partnerships with external organizations.
The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the EMEA region. Key responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports to mitigate risks and ensure regulatory adherence.
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. You will evaluate compliance with GMP, regulatory requirements, and quality systems, and provide sterile manufacturing expertise. The role requires strong communication and stakeholder engagement skills.
This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing a global medical team, managing external partnerships, and ensuring scientific quality and compliance.
This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing global medical teams, managing external partnerships, and ensuring scientific quality and compliance.
