Biotechnology Jobs

• 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 days in office
• US$284,250 – US$473,750 pa
• Director · manages people

Leads a team of medical directors and clinical scientists designing and executing early-phase oncology trials, including first-in-human and proof-of-concept studies, while bridging preclinical discovery and clinical development. Accountable for clinical development plans, translational and biomarker strategy, and regulatory submissions across a lung and head/neck cancer portfolio.

AI/ML

• Waltham, United States
• Hybrid · 2–3 days in office
• US$222,750 – US$371,250 pa
• Director

Serves as the physician on oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation across Phase I–III studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2–3 days per week.

AI

• Stevenage
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, regulatory interactions and investigator engagement, with on-site presence 2-3 days per week.

AI-enabled insights

• Zug, Switzerland
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation. Partners with the Senior Scientist and cross-functional teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2-3 days per week.

AI-enabled insights

• London
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation across Phase I–III studies. Partners with Senior Scientists and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2–3 days per week.

AI

• Mississauga, Canada
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within oncology clinical programme teams, leading medical monitoring and safety oversight for lung and head/neck cancer studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators, regulators and cross-functional matrix teams across Phase I–III development.

• London
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development of oncology assets in genitourinary cancers, overseeing Phase 1-3 interventional trials from protocol design through final study report. Provides real-time medical monitoring, safety review with pharmacovigilance, and regulatory document authoring, while building relationships with key external experts. Serves as a core member of the Clinical Matrix Team and contributes to disease area strategy and business development diligence.

• Waltham, United States
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development of GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds relationships with key external experts and represents the company at advisory boards and medical meetings.

• Stevenage
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development of GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds external expert relationships and represents the company at advisory boards and medical meetings.

• Zug, Switzerland
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development for GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds external expert relationships and represents the company at advisory boards and medical meetings.

• London
• Hybrid · 2 days in office
• US$202,500 – US$371,250 pa
• Director · manages people

Leads clinical development strategy for hepatology assets within GSK's Respiratory, Immunology & Inflammation Research Unit, from target identification through proof-of-concept studies. Accountable for clinical matrix team leadership, protocol design, medical monitoring and regulatory interactions across all development phases. Hybrid role with at least two on-site days weekly.

• Boston, United States
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director · manages people

Leads clinical development strategy for hepatology assets within the Respiratory, Immunology & Inflammation Research Unit, overseeing study design, medical monitoring, and regulatory interactions. Accountable for the Clinical Matrix Team, target validation, translational plans, and Go/No Go decision criteria across early-phase programs. Hybrid role requiring on-site presence at least two days per week.

• Stevenage
• Hybrid · 2 days in office
• US$202,500 – US$371,250 pa
• Director · manages people

Leads clinical development strategy for hepatology assets within the Respiratory, Immunology & Inflammation Research Unit, identifying next-generation liver disease targets and progressing them to proof-of-concept. Accountable for clinical development plans, study protocols, medical monitoring and safety governance, and chairs the Clinical Matrix Team. Hybrid role with at least two days per week on-site.