Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid
• Director

Senior individual-contributor role building a cardiovascular and cardiometabolic translational biology strategy within a respiratory and immunology research unit. Involves defining human-relevant mechanistic hypotheses, biomarker strategies, target evaluation, and business development diligence, with matrix influence across clinical, genetics, and portfolio teams.

• London
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation and sample handling. Manages project plans, budgets and timelines while engaging diagnostic companies, clinical labs and vendors, and supporting regulatory submissions. Works cross-functionally with research, clinical, regulatory and commercial teams in a hybrid model.

FDA · EU IVDR · PMDA +2

• Oxford
• On-site
• Permanent

Develops and scales experimental platforms to test engineered protein variants for photosynthetic efficiency, photoprotection and carbon assimilation. Combines transient plant expression, molecular biology and high-throughput photosynthetic phenotyping, working with computational scientists and protein engineers to inform go/no-go decisions for crop transformation.

• Oxford
• On-site
• Senior
• Permanent

Designs and engineers plant specialised metabolism in cell cultures to produce high-value natural products for health and medicine, applying synthetic biology to optimise biosynthetic pathway flux and product tolerance. Works with AI and robotics teams on model-driven engineering and stage-gated milestones, with a focus on IP generation and translating research into commercial solutions.

• Cambridge
• £74,250 – £202,125 pa
• Lead

Joins the Genomic Technologies group within Translational Sciences, working in an existing Statistical Genetics team. Develops and tests production implementations of methods for large-scale genetic data analysis, 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.

Python · R · SQL +6

• USA - Pennsylvania - Upper Providence
• US$121,275 – US$202,125 pa
• Lead

Joins the Genomic Technologies group within Translational Sciences, working in an existing Statistical Genetics team on large-scale human genetic data. Develops and tests production methods for genetic analysis, integrates multi-omic and phenotypic data to find causal gene-phenotype links and drug targets, and collaborates with biostatistics, AI/ML and disease research teams.

SQL · PySpark · BigQuery +4

• London
• Hybrid · 2–3 days in office
• Senior

Embedded forward deployed engineer role in GSK's Enterprise AI team, working within the Chemical Manufacturing & Control area to prototype AI solutions at days-to-weeks cadence. Focuses on document authoring and generation for regulatory filings, agentic workflows, RAG, knowledge systems and LLM evaluation, with heavy daily use of AI coding agents. Proven prototypes are handed off to a Sr. Solutions Engineer for scale-up.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

• Stevenage
• Hybrid · 2–3 days in office
• Senior

Embedded with CMC business teams, you take high-priority AI use cases from problem framing to working prototypes at days-to-weeks cadence, then ship first production versions. The work centres on document authoring and generation for regulatory filings, building agentic and RAG pipelines, human-in-the-loop review workflows, and LLM evaluation with golden datasets and regression testing.

Claude Code · GitHub Copilot · Databricks AI Assistant +5

• London
• Hybrid · 2–3 days in office
• US$187,275 – US$312,125 pa
• Director

Leads the scientific design and execution of interventional clinical studies within Medical Affairs, providing medical governance, safety data review and scientific oversight of protocols and analysis plans. Collaborates with cross-functional teams, investigators and thought leaders, and presents results for publications and regulatory submissions. Hybrid role with two to three days per week in office.

Digital Tools

• Waltham, United States
• Hybrid · 2–3 days in office
• US$187,275 – US$312,125 pa
• Director

Leads the scientific design and execution of interventional clinical studies within Medical Affairs, providing medical governance, safety data review and scientific oversight of protocols and analysis plans. Collaborates with cross-functional teams, investigators and thought leaders, and presents results for publications and regulatory submissions. Hybrid role with two to three days per week in office.

• Waltham, United States
• Hybrid
• US$204,000 – US$340,000 pa
• Director

Leads the design and execution of real-world evidence and health outcomes studies for oncology assets, managing timelines, budgets and quality of protocols, analyses and publications. Advises internal medical, market access and commercial teams and external experts on evidence strategy for HTA submissions, reimbursement and value-based pricing. Requires close collaboration across a matrix and deep knowledge of real-world data sources and payer needs.

• London
• Hybrid
• US$204,000 – US$340,000 pa
• Director

Leads the design and execution of real-world evidence and health outcomes studies across oncology assets, managing timelines, budgets and quality of protocols, analyses and publications. Advises internal medical, market access and commercial teams and external experts on evidence strategy for HTA submissions, reimbursement and value-based pricing, while building knowledge of real-world data sources and payer needs.

• Rockville Tower Oaks Blvd
• Hybrid
• US$204,000 – US$340,000 pa
• Director

Leads the design and delivery of real-world evidence and health outcomes studies across oncology assets, managing protocols, budgets, timelines and vendor deliverables. Partners with medical, market access, R&D and commercial teams plus external experts to shape evidence for HTA submissions, reimbursement and value-based pricing. Requires deep knowledge of RWD sources and payer evidence requirements.

• Durham Blackwell Street
• Hybrid
• US$204,000 – US$340,000 pa
• Director

Leads the design and delivery of real-world evidence and health outcomes studies for oncology assets, managing protocols, budgets, vendors and reporting from concept to publication. Advises medical, market access and commercial teams on payer and HTA evidence needs, and builds relationships with external experts and data partners.

• Waltham, United States
• Hybrid · 2–3 days in office
• Director · manages people

Leads end-to-end clinical development of hematology oncology assets from first-in-human studies through registrational trials, regulatory approval and launch. Sets disease-area strategy, chairs governance forums and scientific advisory boards, and line-manages clinical development leads and medical directors within a global matrix team.

AI/ML