Joins the Genomic Technologies group within Translational Sciences, working in an existing Statistical Genetics team on large-scale human genetic data. Develops and tests production methods for genetic analysis, integrates multi-omic and phenotypic data to find causal gene-phenotype links and drug targets, and collaborates with biostatistics, AI/ML and disease research teams.
Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability and chairing a cross-functional matrix Medicine Development Team spanning clinical, translational, regulatory, manufacturing and commercial. Drives strategy, go/no-go decisions and lifecycle plans for novel vaccine platforms such as mRNA and neoantigen-based therapies.
Develops and implements bioinformatics algorithms for genomic and transcriptomic analysis, applying machine learning to predict complex traits and phenotypes from large-scale plant datasets. Works within a bioinformatics platform team, collaborating with engineers and research scientists to integrate algorithms into production pipelines and translate research questions into analytical milestones.
Develops and scales experimental platforms to test engineered protein variants for photosynthetic efficiency, photoprotection and carbon assimilation. Combines transient plant expression, molecular biology and high-throughput photosynthetic phenotyping, working with computational scientists and protein engineers to inform go/no-go decisions for crop transformation.
Servicing, installing, repairing and calibrating laboratory diagnostics systems in pathology departments, NHS labs and clinical chemistry sites, including flow cytometry and cell separation products. Field-based customer-facing work on sophisticated electro-mechanical and electronics equipment, backed by a strong R&D-led manufacturer.
Servicing, installing, calibrating and repairing sophisticated laboratory diagnostics systems in pathology departments, NHS labs and clinical chemistry sites, including flow cytometry and cell separation products. Field-based, customer-facing role requiring an electronics or electro-mechanical service background and ONC/HNC-level qualification.
Leads model-informed drug development for oncology programmes, defining and executing model-based strategies from late candidate selection through life cycle management. Conducts population PK, exposure-response and simulation-based trial design work, applying AI/ML and quantitative systems pharmacology methods, and defends results to governance boards and regulators. Sits within a matrixed Clinical Pharmacology Modelling and Simulation group working across small molecules, biologics and antibody drug conjugates.
Leads respiratory epidemiology and real-world evidence programs that inform vaccine development, accountable for at least one asset or disease area and its Global Epidemiology Plan. Designs and oversees complex observational studies using claims, EHR and registry data, advises clinical, safety and regulatory matrix teams, and manages external partnerships and scientific dissemination. Also mentors junior epidemiologists and represents the company with regulators and at international conferences.
Leads respiratory epidemiology and real-world evidence programs that inform vaccine development, designing and overseeing complex studies on disease burden, treatment patterns and safety. Partners across clinical development, safety, regulatory and health outcomes, manages external collaborations, and mentors junior scientists. Hybrid role requiring on-site presence at least two days per week.
Leads respiratory epidemiology and real-world evidence programmes that inform vaccine development, designing and overseeing complex studies on disease burden, treatment patterns and safety. Partners with clinical development, safety, regulatory and external collaborators, and mentors junior staff. Requires deep RWE and pharmaco-epidemiology expertise in a global, matrixed environment.
Leads respiratory epidemiology and real-world evidence programs that inform vaccine development, owning the epidemiology plan for at least one asset or disease area. Designs and oversees complex observational studies using claims, EHR and registry data, advises clinical, safety and regulatory teams, and manages external partnerships while mentoring junior scientists.
Accountable for the strategic execution and coordination of internal and external Real World Data platform partnerships, ensuring maximum scientific value from RWD across R&D and portfolio activities. Leads above-therapy-area data partnerships, informs data linkage and governance strategy, and partners with engineering, AI and DevOps teams on pipeline and infrastructure. Distinct for its global, cross-functional scope spanning translational sciences, medical affairs and commercial functions.
Leads strategic execution of internal and external real-world data platform partnerships to support R&D and portfolio decision-making, spanning multiple geographies and health systems. Coordinates data acquisition, governance, linkage and evidence generation with engineering, AI, DevOps and therapy-area teams, and maintains the RWD asset inventory and partnership KPIs.
Leads the strategic execution of external real-world data partnerships to support R&D and portfolio decision-making, aligning data acquisition with pipeline strategy across therapy areas. Acts as Business Data Owner for RWD assets, stewarding investment governance, data quality and compliance, and working with legal, procurement, data platforms and AI engineering teams to deliver research-ready, FAIR data products.
Leads the strategic execution of external Real World Data partnerships to support R&D and portfolio decision-making, working with clinical, medical and RWE leaders to assess scientific value. Stewards investment governance, manages a portfolio of RWD and external cohorts, and partners with legal, procurement, data platforms and AI engineering teams to ensure research-ready, compliant data products.
