56 jobs within 10 miles of Stevenage
Provides scientific and medical expertise at study level across early- and late-phase hepatology assets, leading protocol and study document development, serving as medical monitor for Phase 1-4 trials, and interpreting efficacy, safety and biomarker data. Works within cross-functional global study teams and mentors less experienced clinical scientists without formal line management.
Owns operational delivery of diagnostics across early and late-stage oncology trials, covering biosample collection, processing and storage, and implementation of clinical trial assays at reference and central labs and CROs. Works in a matrix with biomarker, clinical operations, data management, regulatory and procurement colleagues, managing vendors, contracts and data transfer agreements while keeping studies audit-ready.
Autolus · 101–500 people · Series C
Accountable for onboarding and ongoing performance management of apheresis and treatment centres supporting clinical and commercial CAR T-cell therapies across the UK and Rest of World. Serves as the technical operations single point of contact, conducting site assessments, training centre staff, supporting quality systems and deviations, and managing process change rollouts. Involves up to 50% travel and possible management of contract employees.
Electronic Data Management Systems
Autolus · 101–500 people · Series C
Hands-on manufacturing role producing autologous cell therapies, with roughly 85% of time spent in a GMP cleanroom operating cell-processing equipment, completing documentation and supporting environmental monitoring. Two levels are open: an entry-level Associate Operator and an Operator I for those with GMP or cleanroom experience who take on cell culture, sampling and drug product inspection duties.
GMP Cleanroom · Cell-Processing Equipment
Provides safety science and pharmacovigilance support across the Roche portfolio, covering signal detection, benefit-risk assessment, ICSR case management and aggregate reporting such as DSUR and PBRER. The role also involves preparing CCDS, labelling, RMP and REMS documents and shaping drug safety input into clinical development strategy. Level is set by experience, working with a global team from the Welwyn office.
DSUR · PBRER · CCDS +3
Serves as the physician on a clinical program team, leading medical monitoring and safety oversight for oncology and hematology studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. May mentor other physicians on complex multi-study programs.
AI
Provides clinical and scientific leadership across early and late-stage respiratory programmes, shaping clinical development plans, study designs and regulatory documents. Leads a cross-functional Clinical Matrix Team, oversees medical monitoring and safety governance, and partners with biology, regulatory, commercial and statistics groups to advance differentiated medicines.
Designs, builds and maintains modular end-to-end data-flows across GSK's R&D division, integrating scattered systems and sources into reusable, machine-readable assets with compliance built into the pipeline. Combines hands-on coding and data specification work with coaching and peer review to raise the team's data-flow standards.
Azure · GCP
Designs, develops and maintains modular end-to-end data-flows across GSK's R&D ecosystem, turning scattered systems and sources into trusted, reusable, machine-readable assets. Embeds compliance-as-code and governance into pipelines, working with metadata ecosystems and agentic solutions on Azure or GCP, and coaches peers on data-flow best practice.
Azure · GCP
GSK · 10000+ people · Public
Leads the design and execution of clinical biomarker and translational medicine strategies for late-stage oncology assets, defining predictive biomarkers, patient segmentation and go/no-go decision criteria. Represents Translational Medicine on Clinical Matrix Teams and works across diagnostics, data sciences and external partners to validate assays and deliver biomarker data packages.
NGS · FISH · PCR +5
GSK · 10000+ people · Public
Leads the global development of a medicine from clinical Proof of Concept to approval in first major markets, acting as single point of accountability. Builds and directs a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance and go/no-go decisions. Hybrid role with at least two days on-site per week.
GSK · 10000+ people · Public
Leads model-informed drug development for oncology programmes, defining and executing model-based strategies from late pre-candidate selection through life cycle management. Conducts population PK, exposure-response and simulation-based trial design work across small molecules, biologics and antibody drug conjugates, applying AI/ML and quantitative systems pharmacology methods. Presents and defends modelling outcomes to governance boards and regulators, and contributes to protocols, analysis plans and submissions.
NONMEM · R
Leads Quantitative Systems Pharmacology and QST modelling within GSK's Clinical Pharmacology and Quantitative Medicine group, building mechanistic mathematical models of disease, drug action and trial design. Defines clinical pharmacology strategy across the Respiratory, Immunology and Inflammation portfolio, working with biologists, clinicians, statisticians and AI/ML colleagues. The role sits in a newly formed Centre of Excellence for Model-Informed Drug Development, initially in Stevenage with a planned move to Cambridge.
Leads the development and execution of the analytical (QC testing) network strategy across GSK's global supply chain, translating approved strategy into an operational roadmap and securing endorsement from governance forums such as the Supply Chain Review Board. Drives benchmarking, KPI and reporting frameworks, and capability building across GSC Strategy, with focus on large molecules, ADCs and Oligos.
GSK · 10000+ people · Public
Joins the Genomic Technologies group within Translational Sciences, working in an existing Statistical Genetics team. Develops and tests production methods for analysing large-scale human genetic data, integrating genetic association data across omic and phenotypic layers to identify causal genes, drug targets and biomarkers. Collaborates with Data and Predictive Sciences, Biostatistics, AI/ML and disease area teams to influence portfolio decisions.
PySpark · BigQuery · Docker +3
