Biotechnology Jobs

• Waltham, United States
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programs, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation, and sample collection. Partners cross-functionally with research, clinical, regulatory, and commercial teams, and engages external diagnostic companies and labs to accelerate assay development. Hybrid role based in Waltham, MA.

FDA · EU IVDR · PMDA/MHLW Japan +2

• USA - Pennsylvania - Upper Providence
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials, biomarker selection, assay validation and sample handling. Oversees project plans, budgets and regulatory submissions while managing external diagnostic partners, labs and vendors in a matrixed cross-functional environment.

FDA · EU IVDR · PMDA/MHLW Japan +2

• Philadelphia, United States
• US$203,775 – US$339,625 pa
• Director

Provides scientific and strategic leadership for real-world evidence supporting an mRNA vaccine portfolio, with a primary focus on influenza. Shapes evidence generation across late-stage development, launch and post-marketing, leading US post-marketing vaccine effectiveness studies and external academic and data-partner collaborations. Requires deep expertise in influenza epidemiology, real-world data and causal methods, plus influence across a global matrix.

Medicare · EHR

• Waltham, United States
• US$203,775 – US$339,625 pa
• Director

Provides scientific and strategic leadership for real-world evidence supporting an mRNA vaccine portfolio, with a primary focus on influenza. Shapes evidence generation across late-stage development, launch and post-marketing, leading US post-marketing vaccine effectiveness studies and complex external collaborations with academic and healthcare data partners.

Medicare · EHR · Administrative Claims +1

• London
• US$203,775 – US$339,625 pa
• Director

Provides scientific and strategic leadership for real-world evidence supporting an mRNA vaccine portfolio, with a primary focus on influenza. Shapes evidence generation across late-stage development, launch and post-marketing phases, leading US post-marketing vaccine effectiveness studies and complex external collaborations with academic and healthcare data partners.

Medicare · EHR · Administrative Claims +1

• Durham, United States
• US$203,775 – US$339,625 pa
• Director

Leads the integrated real-world evidence and health outcomes strategy for mRNA influenza vaccines, designing and interpreting US post-marketing vaccine effectiveness studies across late-stage development, launch and post-marketing phases. Partners with clinical development, epidemiology, medical affairs, regulatory, biostatistics and market access teams, and builds 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 · Administrative Claims +1

• 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

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

Embedded with Chemical Manufacturing & Control teams, you take high-priority use cases from problem framing to working prototypes at days-to-weeks cadence, then hand proven solutions to a Solutions Engineer for scale-up. Work is AI-augmented: agent frameworks, multi-agent orchestration, MCP, and AI coding assistants are the default mode of building, turning manual lab and process workflows into agentic automation.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

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

Embedded with Chemical Manufacturing & Control teams, you take high-priority use cases from problem framing to working prototypes at days-to-weeks cadence, then ship first production versions. Work is AI-augmented: agent frameworks, multi-agent orchestration, MCP and AI coding assistants handle routine coding while you supply judgement and validation, coaching BU engineers along the way.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

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

Embedded with chemical manufacturing teams, you take AI use cases from problem framing to working prototypes at days-to-weeks cadence, building in-silico process models, digital twins and optimization solutions. Work is AI-augmented, with coding agents handling routine development while you supply judgement, validation and model identification. Proven solutions are packaged for handoff to a solutions engineer for scale-up.

Claude Code · GitHub Copilot · Databricks AI Assistant +6

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

Embedded with chemical manufacturing teams, you build in-silico process models, digital twins and optimization solutions, taking proofs of concept to deployed MVPs at a days-to-weeks cadence. Work is AI-augmented, with coding agents handling routine development while you focus on model identification, scenario planning and handing proven solutions to solutions engineers.

Claude Code · GitHub Copilot · Databricks AI Assistant +4

• London
• Director · manages people

Owns the product vision and roadmap for AI-enabled digital products that support structured, collaborative authoring of evidence and regulatory content across clinical, non-clinical, CMC, safety, regulatory and publications. Leads a multi-disciplinary product team, shapes scalable architecture with engineers, and drives an AI-first approach with GxP, privacy and AI governance embedded from the outset.

Cloud · DevOps

• 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

• London
• 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, periodic regulatory reports, RMPs and benefit-risk assessments within a global cross-functional matrix, presenting complex safety issues to senior governance committees. Distinct for its blend of pharmacovigilance strategy, regulatory writing and matrix leadership.

ICH · GVP · CIOMS