Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
Manages clinical trial case management activities, ensuring compliance with international and national regulations including GxP and pharmacovigilance standards. Oversees safety reporting, vendor performance, and case processing for serious adverse events, while acting as a key liaison for inspections and audits. Provides training, supports database enhancements, and ensures accurate coding and consistency in safety data analysis.
This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while guiding cross-functional teams and managing vendor performance. They also support redaction of confidential information and drive process improvements across disclosure operations.
Provides microbiological and environmental monitoring expertise to support aseptic manufacturing and clean room operations in compliance with cGMP standards. Oversees environmental control programs, conducts investigations, supports audits, and ensures regulatory compliance across production and QC facilities. Focuses on maintaining high standards in controlled environments and improving processes for patient safety.
This role involves providing Quality Assurance support for aseptic manufacturing operations, ensuring compliance with GMP and regulatory standards. The specialist will review deviations, batch records, and change controls, while supporting investigations and audits. The position emphasizes technical advice, continuous improvement, and maintaining high-quality standards in cleanroom environments.
As a Specialist Biomedical Scientist in Haematology and Blood Transfusion, you will work across central and satellite laboratories, processing and analysing patient samples, performing complex tests, and maintaining high standards of quality and safety. You will also support junior staff, manage stock, and participate in out-of-hours duties.
This role involves designing and executing biological screening cascades to validate computational predictions in drug discovery. The scientist will lead biophysical, biochemical, and cellular assay development, collaborate with CROs, and bridge AI-driven insights with experimental validation across oncology and immunology programs. Close collaboration with medicinal chemistry, structural biology, and machine learning teams ensures data informs rational drug design.
Lead translational strategies for oncology and immunology programs by designing in vivo pharmacology and PK/PD studies to validate AI-designed drug candidates. Bridge computational predictions with experimental validation through CRO partnerships and biomarker-driven approaches. Drive preclinical data generation to inform clinical trial design and regulatory filings.
This role involves performing routine environmental monitoring, water sampling, and microbiological testing (including sterility, bioburden, and endotoxin) for mRNA products in a GMP-regulated manufacturing environment. The analyst will support method transfers, data review, investigations, and compliance activities while working closely with internal teams and contract laboratories. Emphasis is placed on digital workflows, data integrity, and adherence to cGMP standards.
Designs and leads the implementation of enterprise integration solutions using MuleSoft, focusing on secure, scalable APIs and data pipelines. Works closely with data and application teams to align technical architecture with business needs in a regulated biotech environment. Contributes to data strategy, including MDM and Data Lakehouse initiatives, while ensuring compliance with HIPAA, GDPR, and GxP.
Operate and maintain equipment in a cGMP-compliant, highly automated mRNA vaccine production environment at Moderna's Oxford facility. Perform production operations, support quality assurance, troubleshoot issues, and contribute to continuous improvement initiatives using digital systems and advanced manufacturing technologies. Work within a 2-2-3 rotating shift pattern to ensure reliable, safe, and compliant vaccine manufacturing.
Lead clinical sciences strategy and execution for global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. Focus on immuno-oncology with strong emphasis on regulatory compliance, patient safety, and scientific leadership across clinical development phases. Work within a matrix environment to guide study design, interpretation, and regulatory submissions.
Leads strategic positioning of clinical assets in oncology and immunology, leveraging AI-driven insights from the Recursion OS to inform go/no-go decisions, competitive differentiation, and portfolio prioritization. Works cross-functionally with clinical, platform, and business development teams to align resource allocation and advance transformative medicines. Focuses on integrating mechanistic, biomarker, and market data to build compelling narratives for internal and external stakeholders.
Leads global procurement strategy for GSK's R&D in biopharmaceuticals and antibody drug conjugates, managing a £300M annual spend and a team of 4–6. Focuses on sourcing from CDMOs, negotiating complex contracts, and aligning supplier networks with R&D pipeline needs. Works closely with internal stakeholders and external partners to drive innovation, cost efficiency, and supply chain resilience.
The Master Scheduler, Engineering is responsible for strategic planning and coordination of engineering projects, ensuring efficient resource use and adherence to timelines. This role involves leading cross-functional collaboration, monitoring project progress, mitigating risks, and ensuring compliance with regulatory standards. The position supports the delivery of innovative T cell therapies within a fast-paced biopharmaceutical environment.
Provide high-level executive support to the CEO of a clinical-stage TechBio company, managing a complex calendar, international travel, and communications while serving as a key liaison across global teams and stakeholders. Enable strategic priorities through proactive coordination of board meetings, investor events, and cross-functional initiatives in a fast-paced biotechnology environment. Operate with discretion and precision in a mission-driven organization focused on accelerating drug discovery through AI and industrialized biology.
