58 jobs for “Biotech Research Scientist”
GSK London £123,000 – £205,000 pa
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.
GSK Wavre, Belgium €123,000 – €205,000 pa
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.
EMBL-EBI Saffron Walden £3,452 pm
Maintains microbial genomes in Ensembl, loading new annotations, coordinating releases and diagnosing data issues. Develops functional annotation and pangenome pipelines, evaluates taxon-specific annotation tools, and builds Nextflow or Snakemake workflows with Python, relational databases and HPC or cloud infrastructure.
Thermo Fisher Scientific Manchester
Conducts multiple ongoing clinical trials, handling informed consent, screening, vital signs, ECGs and protocol procedures while ensuring subject safety and accurate data capture. Engages across site operations including recruitment, enrolment and retention, working with research site and interdepartmental teams under FDA/GCP and ICH regulations.
Pfizer New York, United States US$176,600 – US$294,300 pa
Leads global evidence generation strategy for a rare disease therapy, overseeing HEOR studies such as network meta-analyses, economic models, and patient-reported outcomes. Partners with cross-functional teams and country affiliates to support reimbursement and market access, managing vendors and budgets. Requires deep HTA and health economics expertise within a matrix organization.
Pfizer Europe - Any Pfizer Site US$176,600 – US$294,300 pa
Leads global health economics and outcomes research for a rare disease asset, developing evidence generation strategy and HEOR studies such as network meta-analyses, economic models and patient-reported outcomes. Oversees launch deliverables including value dossiers and systematic literature reviews, working with cross-functional and country teams to support reimbursement and patient access.
Randstad Construction & Property London
Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships for Patient Cloud products such as eCOA/ePRO, eConsent and virtual trials. Involves risk assessment, study documentation and milestone tracking, with flexibility needed to work American time zones.
ProTech Recruitment Ltd Dorking £45,000 – £55,000 pa
Owns product quality issues in a fast-paced manufacturing environment, leading root cause investigations and corrective actions using 8D, 5 Whys, Fishbone, FMEA and SPC. Works closely with Engineering, Production and Supply Chain on continuous improvement, defect prevention, new product introduction and engineering change reviews, with ISO 13485 and ISO 9001 compliance in a regulated setting.
CSL Maidenhead
Leads strategic sourcing and evaluation of external innovation opportunities in Haematology, identifying preclinical to Phase 1 assets and shaping early partnering strategies. Sits on the Therapeutic Area Leadership Team, co-leads New Product Opportunity reviews, drives cross-functional due diligence and works with Business Development on deal execution. Hybrid, three days a week at an R&D hub site.
CSL Opfikon, Switzerland
Leads strategic sourcing and evaluation of external innovation opportunities in Haematology, identifying preclinical to Phase 1 assets and shaping early partnering strategies. Sits on the Therapeutic Area Leadership Team, co-leads New Product Opportunity reviews, drives cross-functional due diligence, and works with Business Development on deal execution. Hybrid, three days a week at an R&D hub site.
Recursion Remote Opportunity - United Kingdom £136,500 – £167,200 pa
Lead clinical pharmacology and pharmacometrics strategy across a portfolio of rare disease and oncology programs, serving as the clinical pharmacology lead for regulatory interactions and study design from Phase 1-3. Perform and oversee modeling and simulation with tools such as WinNonlin, Monolix, NONMEM and R, and author regulatory sections for IBs, INDs and NDAs. Part of a Pharmacometrics team spanning clinical pharmacology, pharmacometrics and translational modeling, working end-to-end across discovery and development.
Isomorphic Labs Cambridge, United States
Lead and execute the translational medicine strategy for an oncology portfolio, ensuring clinical biomarker assay readiness and data delivery to inform mechanism of action, resistance and future indications. Serve as a core program team member and cancer biology expert, collaborating with AI and computational biology teams to build innovative biomarker analysis tools and advance companion diagnostics.
Recursion Salt Lake City, United States US$200,000 – US$220,500 pa
Lead a team of computational biologists in early discovery, acting as a player-coach who balances hands-on analysis with mentorship. Integrate phenomics, transcriptomics, genomics and proteomics data to nominate oncology and immunology targets, define validation criteria and precision medicine strategies, partnering with biologists, engineers and translational experts.
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 London
Shape global CMC regulatory strategy for an innovative mRNA medicines portfolio, driving international submissions and health authority interactions. Prepare and review CMC sections of regulatory filings, advise Manufacturing and Quality teams, and oversee multiple development programs. An individual contributor role with global reach, working alongside teams using digital and Generative AI tools.
