Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...
This role involves leading 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. The role requires deep scientific expertise and a strong network within biotech, academia, and pharma BD organizations.
This role involves managing technology transfer projects for external drug product manufacturing with Contract Manufacturing Organisations (CMOs). The specialist will coordinate cross-functionally across Procurement, Quality, Technical, and Supply teams to establish and maintain project schedules, mitigate risks, and ensure timely delivery of assets within budget. The position emphasizes strong stakeholder engagement, governance, and retention of manufacturing knowledge across the supply network.
Lead a technical team at GSK’s Ware manufacturing site to monitor and improve product performance across respiratory and oral solid dose medicines. Drive the local execution of the technical lifecycle plan, lead investigations into manufacturing issues, and implement process improvements using lean methodologies and digital tools. Collaborate with global MSAT stewards and site leadership to ensure compliance, efficiency, and innovation in a highly regulated environment.
Leads national medical strategy for cardiovascular, renal, and metabolic therapies, shaping policy, driving NHS collaborations, and accelerating patient access to innovative treatments. Champions real-world evidence, scientific launch readiness, and cross-functional medical execution across the UK healthcare system.
This role involves leading the national medical strategy for respiratory and immunology therapies within the UK NHS landscape, focusing on transforming patient care pathways and accelerating access to innovative treatments. The individual will drive pre-launch and launch readiness initiatives, shape real-world evidence generation, and collaborate with cross-functional teams and external stakeholders including NICE and MHRA. Leadership of field medical teams and strategic input into regulatory, market access, and digital health initiatives are central to the position.
This role involves leading the execution of Moderna's strategic partnership with the UK government, focusing on mRNA-based vaccines and biomanufacturing. You will manage day-to-day interactions with key government stakeholders, represent Moderna on the UKHSA operations board, and drive cross-functional collaboration to deliver public health impact.
The Role:Reporting to the Director, Business Analytics & Operations Management, the Associate Director, Business Analytics & Insights, Clinical Operations will be accountable for development and implementation of analytical & financial systems & tools and processes to perform business analytics within...
This role involves leading the global health outcomes function at ViiV Healthcare, focusing on evidence generation to support HIV treatment and prevention medicines. Responsibilities include strategic leadership, team management, and collaboration with various stakeholders to ensure credible and decision-relevant evidence for patient access and value demonstration.
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 successful collaborations.
The SERM Scientific Director role involves leading pharmacovigilance and risk management strategies for clinical development and post-marketing products. Responsibilities include evaluating safety data, managing safety concerns, and supporting regulatory activities. The role operates in a global, cross-functional environment and may include mentoring responsibilities.
This role involves developing and delivering robust regulatory strategies for oncology products, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation in regulatory affairs.
This role involves developing and delivering robust regulatory strategies for drug development and approval, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation within the regulatory framework.
The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.
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.
