Biotechnology Jobs

• Durham Blackwell Street
• Hybrid · 2–3 days in office
• US$138,600 – US$231,000 pa
• Director

Develops and executes global and regional regulatory strategies for assigned assets in respiratory, immunology and inflammation, managing regulatory interactions, submissions and review processes across major markets. Ensures compliance with internal GSK processes and regulatory requirements to deliver optimal labelling, working in a matrixed team and liaising with commercial and global counterparts.

AI

• Ware
• On-site
• Senior

Embedded on-site at GSK's Ware manufacturing site, acting as the interface between local business teams and global digital product teams. Builds and validates AI, data and Smart Manufacturing proofs of concept, value and MVPs using real site data, then hands proven solutions to product teams for scale-up.

ERP

• 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

• USA - Pennsylvania - Upper Providence
• Hybrid
• Lead

Lead programming activities for complex and pivotal clinical studies, developing, maintaining and validating analysis packages while ensuring compliance with Good Programming Practices and CDISC standards. Mentor junior programmers, support regulatory interactions with EMA and FDA, and bridge scientific requirements with technical solutions in an agile, squad-based global team.

R

• 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)

• Zug, Switzerland
• 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 interaction. Serves as a senior member of the Clinical Matrix Team, mentoring Medical Directors and engaging external experts, with a minimum two-day on-site office presence.

Real World Evidence

• Stevenage
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director

Accountable for end-to-end clinical development of a multi-tumor oncology asset, from first-in-human through registrational trials, regulatory approval and initial market launch. Acts as senior clinical representative at governance forums and leads cross-functional, matrixed teams spanning research, precision medicine, medical affairs and commercial. Requires deep antibody-drug conjugate and global health authority experience.

AI/ML