14 jobs
Alloy Therapeutics UK Ltd Cambridge £45,000 – £50,000 pa
Design and build large-scale synthetic gene loci and transgenic platforms for antibody discovery, using CRISPR/Cas9, RMCE and site-specific integrases. Hands-on molecular biology including PCR, NGS, plasmid construction and flow-cytometric immunophenotyping, within a small multidisciplinary team working from dry-lab design to wet-lab validation.
CureAge Therapeutics London
Lead the computationally guided design of a lipid nanoparticle delivery platform, applying chemical and biophysical principles to optimise LNP composition and formulation. Use AI-enabled chemistry, cheminformatics, predictive models and molecular modelling to prioritise formulation components, working closely with the experimental team and founding team in a small start-up.
Bristol Myers Squibb Uxbridge
Leads EU regulatory strategy for an immunology and cardiovascular portfolio, from early development through registration and lifecycle management. Acts as the regulatory lead for assigned development teams, negotiating with the EMA and other health authorities and building integrated submission plans. Integrates scientific, medical, legal and business perspectives while monitoring European regulatory trends.
Bristol Myers Squibb Uxbridge
Serves as primary medical accountability for multiple Phase 1-3 clinical trials in GI oncology, leading medical data review, safety assessment and site interactions within a Study Delivery Team. Partners with Clinical Scientists on protocol design, benefit/risk analysis and health authority interactions, while building relationships with principal investigators and thought leaders.
Carbometrics Bristol £60,000 – £70,000 pa
Lead the development of a signal-processing pipeline that turns raw optical sensor measurements into reliable analytical results, covering filtering, noise removal, bias compensation and calibration. The hands-on technical leadership role focuses on algorithms rather than product software or UI, working with scientists and engineers in a multidisciplinary team. It starts without line management but offers the chance to build a team as the company grows.
Eurofins Liverpool
Perform routine, non-routine and stability testing on finished pharmaceutical products at a client site, using HPLC, Dissolution, Karl Fischer and UV techniques. The role also covers technology transfers, analytical validation, GMP data review and OOS investigations, working within a managed services team embedded at the client's facility.
Eurofins Liverpool
Perform method development and proof-of-concept validation on pharmaceutical raw materials, intermediates and drug substances, mainly APIs, using HPLC, GC and MS. Support technology transfers for novel substances, review data for compliance, investigate OOS/OOE results and document work to client procedures. Based on-site at a client facility as a managed PSS scientist, liaising with client representatives and supporting audits and continuous improvement.
Bristol Myers Squibb Uxbridge
An individual contributor role conducting non-interventional real-world data research for medical and HEOR teams across international markets. You will identify data sources, oversee statistical programming in R, and interpret and present findings to stakeholders. The position requires deep expertise in observational data analysis and offers hybrid working from Uxbridge.
Bristol Myers Squibb Uxbridge
Serves as primary medical accountability for Phase 1–3 clinical trials in neuroscience, leading medical monitoring, safety assessment and benefit/risk analysis within a matrixed study delivery team. Partners with clinical scientists on protocol design, site interactions and health authority submissions, and builds relationships with principal investigators and thought leaders.
Bristol Myers Squibb Uxbridge
Technical lead on assigned clinical studies, shaping SDTM strategies from protocol review through to global regulatory submission. Involves root cause analysis, cross-functional collaboration, data integration from CRF and non-CRF sources, and engagement with SDTM automation, metadata-driven processes and agentic AI workflows. Also provides quality oversight to team members and manages CRO and vendor programming activities.
Bristol Myers Squibb Uxbridge
Lead statistical programming for clinical trials, turning complex data into submission-ready outputs using SAS, CDISC, and ADaM standards. Embedded in cross-functional teams, you'll review analysis plans, shape programming strategy, and mentor other programmers while supporting major regulatory filings.
Bristol Myers Squibb Uxbridge
Provides scientific and clinical expertise for a cardiovascular therapy area, driving UK medical strategy, research plans and field tactical activities alongside the Field Medical Manager. Manages publications, supports Health Technology Assessment work and acts as a nominated medical signatory, with around 15% national and international travel.
Bristol Myers Squibb Uxbridge
Leads clinical strategy and execution for one or more GI oncology indications of a given asset, owning the Target Product Profile and disease area strategy. Manages a team of physicians and scientists designing, running, analysing and interpreting all clinical studies, and acts as internal and external clinical authority for regulatory interactions and business development. Requires deep therapeutic expertise and 8+ years of drug development experience, with international and domestic travel.
Bristol Myers Squibb Uxbridge
As a senior individual contributor in the Global Biometrics & Data Sciences function, you write and validate SAS programs to produce derived analysis datasets and clinical Tables, Figures and Listings, and contribute to electronic submission packages such as NDA, BLA and MAA. You also review Statistical Analysis Plans and Data Presentation Plans, partner with external vendors on programming standards, and independently lead programming assignments across multiple projects.
Bristol Myers Squibb Uxbridge
As a member of cross-functional development teams, you will contribute to trial design, protocol development, analysis planning, and regulatory submissions. The role involves authoring statistical analysis plans and clinical study reports, defending protocols at governance reviews, and providing statistical leadership on health authority requests. It requires 50% onsite presence in Uxbridge and offers the chance to support a specific asset indication.
Bristol Myers Squibb Uxbridge
Serves as scientific authority for clinical studies across an assigned asset or indication, from protocol development through CSR review and regulatory submission. Leads clinical oversight of study data with Data Management and Programming, may act as Trial Lead on complex global studies, and presents to investigators, KOLs and senior leadership. Also supports process improvement, training and mentoring within the Clinical Capabilities function.
