Biotechnology Jobs

• London
• Hybrid · 2 days in office
• US$284,625 – US$474,375 pa
• Director · manages people

Leads clinical development medical activities for cardiovascular and vascular programs across early and late-phase studies, shaping clinical development plans, study designs and translational strategies. Serves as clinical lead for a matrix team, providing medical monitoring, regulatory input and safety oversight while working with biology, regulatory, commercial and operations colleagues.

• London
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director

Provides clinical and scientific leadership across cardiovascular clinical development programmes, shaping study designs, translational plans and regulatory documents within the Respiratory, Immunology & Inflammation Research Unit. Leads a Clinical Matrix Team, oversees participant safety and medical monitoring, and works cross-functionally with biology, regulatory, statistics and commercial partners. Hybrid working with at least two days per week on-site.

• United Kingdom
• Remote
• Director · manages people

Senior physician role leading medical science and strategy for oncology across a clinical research business, shaping RFP responses, bid defences and protocol design while engaging client medical leadership. Also provides therapeutic training, mentoring and regulatory document input, working in a matrixed global team with international travel.

• Uxbridge
• Director

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.

• New York, United States
• Hybrid · 2–3 days in office
• US$124,400 – US$207,400 pa
• Lead · manages people

Leads the strategy, design and lifecycle management of Pfizer's clinical supply chain systems, aligning a 3-5 year product roadmap with Global Clinical Supply objectives. Partners with digital product managers and business SMEs on solution design, process improvement and portfolio prioritisation, reporting metrics to senior leadership. Hybrid role with up to 15% travel.

• Leeds
• Director · manages people

Owns product strategy, roadmap and innovation for clinical pharmacology clinics and bioanalytical labs, spanning early-phase platforms like ClinSpark, LIMS/LIS, ELN, instrument connectivity and lab automation. Builds business cases and secures funding, governs a regulated portfolio, and leads multidisciplinary product teams and vendors across distributed sites.

ClinSpark · LIMS · LIS +7

• Manchester
• Mid-level

Monitors clinical trial sites through selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines, while driving subject recruitment and tracking regulatory submissions, CRF completion and data queries. Works within a full-service, multi-sponsor site management team, training site staff and maintaining Trial Master File documentation.

• United Kingdom
• Remote
• Senior

Monitors investigator sites using a risk-based approach, conducting remote and on-site visits to assess protocol and regulatory compliance, performing SDR, SDV and CRF review, and documenting findings in reports. Acts as a site processes specialist ensuring trials follow ICH-GCP, applicable regulations and SOPs, while developing collaborative relationships with investigational sites and supporting audit readiness.

CTMS · Microsoft Office

• Cambridge
• Director · manages people

Leads a team of medical writers and oversees strategic planning and drafting of complex regulatory submissions at the therapeutic area or portfolio level. Acts as subject matter expert, driving document strategy with cross-functional teams across Regulatory Affairs, Clinical Research and Clinical Data Science, plus process improvement and training initiatives.

Workday

• Sheffield
• £39,560 – £48,337 pa
• Entry level
• Contract

Lead the design, assembly and clinical validation of a novel dialyser prototype within the Thermofluids Group, testing with blood-mimicking fluids and human blood to assess cleaning efficiency, clotting risk and biocompatibility. Work alongside two other Research Associates covering numerical simulation and experimental fluid dynamics, in collaboration with the Medical School and Sheffield Teaching Hospitals.

• Exeter
• £21,805 pa
• Entry level
• Contract

An interdisciplinary PhD studentship combining computational genomics at Exeter with stem-cell biology and CRISPR editing at Cambridge. The student will analyse whole-genome sequencing data from large multi-ancestry cohorts, integrate genetic signals with epigenetic maps and AI tools like AlphaGenome, and build iPSC-derived visceral and subcutaneous adipocyte models to functionally test prioritised regulatory variants.

AlphaGenome · DNANexus · Flow Cytometry +1

• Exeter
• £21,805 pa
• Entry level
• Contract

Applies genetic clustering to severe mental illness traits to find biologically distinct risk components affecting obesity and type 2 diabetes, using GWAS data and population biobanks. Integrates single-cell multiomic datasets to map risk pathways to neuronal and glial cell types, with CRISPR-based functional work. Multidisciplinary training in statistical genetics, bioinformatics and functional genomics.

CRISPR · GWAS

• London
• On-site
• Mid-level
• Permanent

Own the full post-training lifecycle for biological foundation models, from alignment strategy to production deployment. Design pipelines that adapt general-purpose models to therapeutic contexts, build validation frameworks linking model improvements to biological ground truth, and run experiments end-to-end on distributed GPU infrastructure. Collaborate with ML infrastructure and biology teams and contribute to open-source tooling.

OpenTargets · helical-package · GPU

• Cambridge, United States
• Hybrid · 3 days in office
• Senior · manages people

Designs and implements translational strategies for small molecule oncology and immunology programs, from early discovery through candidate selection and clinical phase. Oversees CRO activities, PK/PD and safety assessments, and biomarker strategies, bridging computational predictions with laboratory validation. Some roles include managing 2-3 in vivo pharmacologists.

Machine Learning · AlphaFold

• Oxford
• Lead · manages people

Lead a team of scientists developing novel biologic therapies for autoimmune disease, overseeing in vitro and in vivo pharmacology studies for lead and early discovery programs. Collaborate across immunology, protein engineering, translational medicine and biomarkers to deliver data packages for progression to development, while mentoring staff and contributing to INDs and patents.