104 jobs for “Biotech Research Scientist”
Isomorphic Labs London
Lead the hardening and scaling of an inference platform serving fleets of cutting-edge ML models for scientific applications. Set strategy and roadmaps, architect next-generation services to solve scaling limits, and partner with research, product and operations teams to align infrastructure with biotech R&D cycles.
Isomorphic Labs London
Lead all externalised drug discovery and preclinical lab operations, building and scaling a global CRO infrastructure for an AI-first drug design platform. Oversee experimental throughput, data QC and turnaround times, embed data-generation-by-design standards, and manage vendor governance, budgets and a team of CRO Scientific Leads, Operations Managers and Compound Managers.
GSK London
Builds and maintains financial and operational models, forecasts and dashboards that guide R&D portfolio and investment decisions, including NPV/rNPV, scenario and sensitivity analysis and Monte Carlo simulation. Works with the Head of Data Science and the Finance Portfolio Analytics Manager, turning scientific, clinical, financial and operational data into clear outputs for review discussions.
GSK USA - Pennsylvania - Upper Providence
Builds and maintains financial and valuation models (NPV/rNPV, scenario and sensitivity analysis) and portfolio forecasts, metrics and KPI dashboards for R&D investment decisions. Runs probabilistic and Monte Carlo simulations, cleans data from scientific, clinical, financial and operational sources, and prepares decision materials for portfolio reviews. Works with the Head of Data Science and the Finance Portfolio Analytics Manager in a hybrid, high-visibility team.
CSL Maidenhead
Leads an integrated quality assurance organisation covering Good Clinical Practice and Good Pharmacovigilance Practice, reporting to the Head of Global R&D Quality. Sets strategy, operating model and standards for risk-based QA oversight from trial design through close-out, including clinical safety interfaces, inspection readiness and CAPA frameworks. Hybrid role with global scope and international travel.
CSL Waltham, United States
Leads an integrated quality assurance organisation covering Good Clinical Practice and Good Pharmacovigilance Practice, reporting to the Head of Global R&D Quality. Sets strategy, operating model and standards for risk-based QA oversight from trial design through close-out, including inspection readiness, CAPAs and clinical safety interfaces such as SAE reconciliation and expedited reporting. Hybrid role with global team leadership and international travel.
Recursion New York, United States US$151,800 – US$220,660 pa
Integrates phenomics, transcriptomics, genomics and proteomics data to nominate and validate oncology targets and define precision oncology patient strategies. Partners cross-functionally with biologists, chemists, engineers and translational experts to build target data packages and pilot novel discovery methods, including agentic target packages and mechanism-of-action work.
Newton Colmore Cambridge
Lead the design and development of next-generation drug delivery devices, guiding multidisciplinary teams of engineers, scientists and designers from early-stage concepts through to manufacturable solutions. The role blends hands-on R&D work — concept generation, prototyping, experimental design, verification planning and risk management — with client-facing consultancy, programme leadership and mentoring of junior colleagues.
Moderna London
Leads CMC regulatory strategy for global submissions including IND, CTA, BLA and MAA, and oversees agency correspondence and compliance for mRNA products. Reviews submissions for readiness, drives health authority interactions, and advises manufacturing and quality teams on change controls and regulatory guidance across vaccines, oncology and rare disease programmes.
Moderna Oxford
Provides scientific and hands-on leadership for immunogenicity and ligand binding assay bioanalysis supporting mRNA-LNP therapeutic programs, spanning assay development, validation, clinical sample testing and regulatory submissions. Ensures GcLP compliance and partners with cross-functional teams, with opportunities to work alongside data and AI-enabled analytical approaches.
SRG Loughborough £14 – £15 ph
Perform analytical testing for batch release, stability studies and complaint investigations in a GMP/GLP-regulated pharmaceutical lab, using techniques such as HPLC and UV spectroscopy. Support OOS/OOT investigations, maintain Good Documentation Practices, review and issue GMP documentation, and help with calibration and equipment maintenance. A 12-month temp contract within a cross-functional QC team.
Autolus London
Designs end-to-end data solutions spanning data integration, data warehousing, master data management, governance and analytics for a biopharmaceutical company. Translates business requirements into data models, data flows and integration patterns, and leads architecture and design reviews across enterprise applications and cloud data platforms.
Vertex Pharmaceuticals London
Leads regional or global regulatory strategy for development programs and marketed products, serving as a regulatory lead and primary contact with health authorities. Manages preparation, submission and approval of regulatory applications, advises teams on approval pathways and expedited routes, and monitors regulatory intelligence to inform strategy.
Genomics London
Client-facing programme manager role setting up and embedding a multidisciplinary delivery team around a major pharma partnership, running the integrated delivery plan, milestones, dependencies, risks and resourcing. Coordinates across Science, Data, Engineering, Finance, Legal and People stakeholders, running status meetings, reporting and escalations with the partner. Structured as a six-month engagement with an immediate start.
Vertex Pharmaceuticals London
Oversees cell and gene therapy Contract Manufacturing Organizations as the primary on-site point of contact, providing operational, quality and technical oversight of cGMP commercial supply. Acts as a Person-in-Plant and SME within the Virtual Plant Team, managing deviations, change controls, batch data and supplier governance, with up to 50% travel and shift coverage for critical process steps.
