Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director

Serves as the physician within a clinical program team, leading medical monitoring and safety oversight for genitourinary oncology studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. May guide other physicians on complex multi-study programs.

AI

• USA - Pennsylvania - Upper Providence
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within an oncology clinical programme team, leading medical monitoring and safety oversight for GI cancer studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators, KEEs and health authorities. A core member of the Clinical Matrix Team, providing medical guidance within a matrixed pharma R&D environment.

AI-enabled insights

• USA - Pennsylvania - Upper Providence
• US$203,775 – US$339,625 pa
• Director

Provides scientific and strategic leadership for real-world evidence supporting GSK's mRNA vaccine portfolio, with a primary focus on influenza. Leads post-marketing vaccine effectiveness studies in the US, translating evidence needs into rigorous study designs and building collaborations with academic investigators, healthcare systems and data partners. Requires deep expertise in US vaccine effectiveness research, influenza epidemiology, real-world data and causal methods.

Medicare · EHR

• Philadelphia Walnut Street
• US$95,700 – US$159,500 pa
• Mid-level

Mid-level individual contributor on GSK's Enterprise AI Forward Deployed Engineering team, embedded with business unit teams to prototype AI proofs of concept at a days-to-weeks cadence. Works under senior FDEs using AI coding assistants and multi-agent workflows as the default mode of building, then hands proven solutions off cleanly to Solutions Engineers for productionisation.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

• London
• Director · manages people

Leads global medical writing for the Respiratory, Immunology and Inflammation portfolio, directing strategy, resourcing and delivery of regulatory-compliant clinical documentation to accelerate submissions. Drives innovation and digital/AI adoption, manages vendor oversight and talent development, and partners with senior R&D stakeholders on governance and process improvement.

AI · Content Management Systems

• Cambridge
• US$205,425 – US$342,375 pa
• Lead · manages people

Senior technical authority leading GSK's Forward Deployed Engineering function, setting enterprise standards for AI-native development while owning delivery outcomes for a portfolio of strategic business units. Stays hands-on across architecture, ML and agentic engineering, leading Staff and Senior FDEs on precedent-setting engagements and acting as escalation point for the hardest technical decisions.

Claude Code · GitHub Copilot · Databricks AI Assistant +4

• London
• Hybrid
• PLN 419,250 – PLN 698,750 pa
• Director

Provides medical and scientific leadership in pharmacovigilance and risk management for Respiratory, Inflammation and Immunology assets in clinical development. Interprets safety data, detects and escalates signals, and delivers evidence-based benefit-risk recommendations to senior governance. Works in a global cross-functional matrix, representing Safety on clinical teams and with regulators.

• Warsaw, Poland
• Hybrid
• PLN 419,250 – PLN 698,750 pa
• Director

Provides medical and scientific leadership in pharmacovigilance and risk management for Respiratory, Inflammation and Immunology assets in clinical development. Interprets safety data, detects and escalates signals, and delivers evidence-based benefit-risk recommendations to senior governance. Leads Safety Review Teams and represents Safety on cross-functional clinical matrix teams in a global hybrid environment.

• Bengaluru Luxor North Tower
• Director · manages people

Leads global medical writing for the Respiratory, Immunology and Inflammation portfolio, directing strategy, resource planning and vendor oversight to deliver regulatory-compliant clinical documentation. Drives submission acceleration, digital innovation and cross-functional partnerships across R&D, with accountability for talent development and operational excellence.

Content Management Systems

• Siena, Italy
• Hybrid
• €81,750 – €136,250 pa
• Director

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting signals and delivering benefit-risk recommendations. Represents Safety on cross-functional matrix teams and governance committees, and interacts with regulators. Hybrid role based in the UK.

• Warsaw, Poland
• Hybrid
• Director
• Permanent

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting and escalating signals, and delivering benefit-risk recommendations. Represents Safety on cross-functional matrix teams and governance committees, and interacts with regulators and external experts. Hybrid role based in the UK with a global matrix environment.

• London
• Hybrid
• Lead

Lead programming activities for one or more clinical studies, developing, maintaining and validating complex analysis packages to CDISC and Good Programming Practice standards. Act as technical mentor to junior programmers and lead programming support for regulatory interactions with the EMA and FDA. Works in an agile, squad-based team bridging scientific requirements with technical solutions, with R proficiency preferred.

R

• Stevenage
• Hybrid
• Lead

Leads statistical programming for complex and pivotal clinical studies, developing, maintaining and validating analysis packages while ensuring compliance with Good Programming Practices and CDISC standards. Acts as a technical mentor to junior programmers and leads programming support for regulatory interactions with bodies such as the EMA and FDA, working in an agile, squad-based team alongside clinical, statistical and operational stakeholders.

R

• Durham
• Hybrid · 2–3 days in office
• €87,000 – €145,000 pa
• Director

Provides medical and scientific expertise in safety evaluation and risk management for GSK assets across clinical development and post-marketing settings. Leads signal detection, regulatory periodic reports, and benefit-risk assessments while collaborating with cross-functional teams including Clinical Operations, Regulatory, and Biostatistics. Involves presenting complex safety issues to senior governance committees and contributing to global regulatory submissions.

ICH · GVP · CIOMS

• Greater Poland
• Hybrid · 2–3 days in office
• €87,000 – €145,000 pa
• Director
• Permanent

Provides medical and scientific expertise in safety evaluation and risk management for GSK assets across clinical development and post-marketing settings. Leads signal detection, benefit-risk assessment, regulatory periodic reports and RMPs, working within a global cross-functional matrix alongside Clinical Operations, Regulatory and Biostatistics. Distinct for its strong focus on pharmacovigilance governance, safety strategy and scientific writing.

ICH · GVP · CIOMS