Biotechnology Jobs

• London
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with cross-functional partners. Designs, oversees and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, data needs and analysis plans. Manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.

Electronic Health Records · Claims Data · Registries

• USA - Pennsylvania - Upper Providence
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine to advance diagnostic and biomarker development programs, coordinating internal groups and external labs and Dx manufacturers. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations. Hybrid role requiring 2-3 days per week onsite.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• Oxford
• On-site
• Mid-level
• Contract

Design, roll out and maintain an ISO 9001-aligned Quality Management System across a research institute, covering document control, audit programmes and management reviews. The role also involves delivering QMS training and acting as a trusted advisor to programme leaders, on a 12-month fixed term contract.

• Oxford
• On-site
• Director · manages people
• Permanent

Builds and leads a molecular biology and synthetic biology function within a plant science institute, setting technical strategy for high-throughput assays, sequencing-based readouts, CRISPR guide design and multiplex editing. Acts as a responsive core facility, coaching scientists on experimental design and integrating with bioinformatics, tissue culture and phenotyping teams. Combines deep technical direction with people leadership rather than routine bench work.

AI · Automation · Microfluidics +3

• Stevenage
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director · manages people

Provides clinical and scientific leadership across translational and clinical studies within GSK's Respiratory, Immunology & Inflammation Research Unit, with a focus on aging. Leads a Clinical Matrix Team, designs clinical development plans and protocols, and oversees medical monitoring, safety and regulatory interactions. Hybrid working with at least two days per week on-site, initially in Stevenage before a planned relocation to Cambridge, UK.

• London
• Hybrid · 2 days in office
• Director

Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight and clinical data interpretation for genitourinary cancer studies. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, investigator engagement and regulatory interactions, with hybrid working of at least two days on-site per week.

AI

• London
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director · manages people

Provides clinical and scientific leadership across early-phase clinical development programs in GSK's Respiratory, Immunology & Inflammation Research Unit, with a focus on aging research. Leads a Clinical Matrix Team, designs clinical development plans and study protocols, oversees medical monitoring and safety, and represents programs in regulatory interactions. Works cross-functionally with biology, translational sciences, commercial, regulatory and statistics partners.

• Warsaw, Poland
• Hybrid · 2 days in office
• PLN 472,500 – PLN 787,500 pa
• Director

Serves as the physician within an oncology clinical program team, leading medical monitoring and safety oversight for genitourinary cancer studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. Hybrid working with at least two days per week on-site.

AI

• Mississauga, Canada
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director

Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight and clinical data interpretation for genitourinary studies. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, investigator and KEE engagement, and regulatory interactions. May guide other physicians on complex multi-study programmes.

AI

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

Serves as the physician within a clinical programme team, leading medical monitoring and safety oversight for oncology studies and interpreting clinical and safety data. Partners with the Senior Scientist and cross-functional teams on protocol development, regulatory interactions and investigator engagement, with a focus on GI oncology. Requires an on-site office presence two to three days a week.

AI-enabled insights

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

Serves as the physician on a clinical programme team, leading medical monitoring and safety oversight for GI oncology studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators and regulators. Works within a Clinical Matrix Team alongside Clinical Operations, Biostatistics, Regulatory and Pharmacovigilance, with on-site presence 2-3 days a week.

AI

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

Serves as the physician within an oncology clinical programme team, leading medical monitoring, safety oversight and clinical data interpretation for GI studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement. Requires on-site presence 2-3 days a week, with the Stevenage base relocating to Cambridge, UK by early 2029.

AI

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

Senior physician leader providing medical oversight, safety evaluation and clinical data interpretation across sarcoma oncology studies, from protocol design through regulatory interactions. Serves on the Clinical Matrix Team, mentors Medical Directors and engages external experts, with a minimum two days a week on-site presence.

Real World Evidence

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

Senior physician leader providing medical oversight, safety evaluation and clinical data interpretation across sarcoma oncology studies, from protocol design through regulatory interactions. Sits on the Clinical Matrix Team, mentors Medical Directors and engages external experts, KEEs and advisory boards. Requires deep soft tissue sarcoma and osteosarcoma drug development expertise.

GCP · ICH Guidelines · Real World Evidence

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

Senior physician leader providing medical oversight, safety monitoring and clinical data interpretation across sarcoma oncology studies, from protocol design through regulatory interactions. Serves as a senior member of the Clinical Matrix Team, mentoring Medical Directors and engaging external experts, with a minimum two days a week on-site presence.

Real World Evidence (RWE)