Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
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.
This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on safety evaluation in clinical development and post-marketing settings. The Scientific Director will lead cross-functional teams, drive safety governance, and ensure regulatory compliance across international markets. The position requires deep expertise in drug safety, signal detection, and benefit-risk assessment to protect patient safety and support regulatory submissions.
This role involves leading and developing the Front Line QA function at Seqirus Liverpool, ensuring pharmaceutical quality across all products. Responsibilities include providing 24/7 QA coverage, overseeing batch review and IT systems, and ensuring compliance with regulatory requirements. The role holder may also act as a QP, certifying and releasing products to market.
This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.
This role involves leading clinical safety strategy for drug projects across development and post-marketing phases, with a focus on oncology. The Medical Director will evaluate safety data from clinical and pre-clinical sources, contribute to global regulatory submissions, and guide risk management using advanced methodologies like signal detection and Safety Knowledge Groups. Based in Luton with a hybrid working model, the position drives patient safety within a global, science-led environment.
This role involves leading toxicology strategy for oncology drug development, focusing on novel targeted therapies such as Radio Conjugates and Antibody Drug Conjugates (ADCs). The Director will design regulatory and investigative studies, integrate safety data using advanced in vitro, in silico, and in vivo methods, and guide cross-functional teams from discovery through to clinical translation. Emphasis is placed on innovation in safety science, including the use of emerging technologies like organ-on-chip and omics.
This role involves managing the non-clinical aspects of IND submissions, including CMC, DMPK, pharmacology, and tox reporting. You will create and maintain detailed project plans, manage data and document workflows, and coordinate cross-functional teams to ensure regulatory compliance and successful submission.
As a Computational Drug Designer, you will work on cutting-edge drug discovery projects, applying AI and computational chemistry to design novel molecules. You will collaborate with interdisciplinary teams, contribute to scientific proposals, and mentor junior colleagues in a fast-paced, innovative environment.
This role involves developing, optimizing, and validating ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data from clinical samples in compliance with GcLP standards, using platforms like Watson LIMS and electronic lab notebooks. The position emphasizes regulatory compliance, critical reagent management, and collaboration with cross-functional teams to deliver high-quality bioanalytical data for clinical programs.
This role involves designing and optimizing automated laboratory workflows for biomarker testing and sample management within Moderna’s Clinical Biomarker Laboratory. The engineer will lead integration of advanced liquid handling systems, develop data pipelines, and ensure compliance with regulatory standards, while collaborating across digital, operations, and vendor teams to build scalable, AI-enhanced automation platforms.
Develop and apply machine learning models for small-molecule drug design with a focus on protein–ligand interactions, binding affinity, and molecular properties. Collaborate with computational chemists, structural biologists, and medicinal chemists to validate and refine ML-generated hypotheses. Work within a multidisciplinary team to drive innovation in drug discovery using structure-driven approaches and foundation models.
This role involves shaping and driving medical affairs strategy in Nephrology and Rheumatology by translating complex scientific data into actionable insights. The Medical Affairs Partner will collaborate with internal teams and external healthcare experts to support patient outcomes, leveraging deep medical expertise and building scientific partnerships. The position emphasizes strategic initiative leadership and stakeholder engagement within the UK affiliate and global context.
This role involves leading statistical programming activities across clinical programs, ensuring the development and quality control of tables, listings, figures, and analysis datasets. You will oversee external vendors, develop standards and innovative technologies, and support data-driven decision-making in drug discovery.
