Biotechnology Jobs

• Stevenage
• Hybrid
• Director

Leads acquisition, integration and analysis of large-scale cancer multi-omic and clinical datasets to drive translational decisions and support the oncology pipeline. Partners with biologists, clinicians, AI/ML engineers and statisticians, building reproducible data pipelines and informatics infrastructure, with mentoring responsibilities in a hybrid team.

Cloud Platforms

• Stevenage
• Lead

Develops and deploys cheminformatics and machine learning models on large proprietary datasets to guide go/no-go decisions across drug-discovery programmes. Embeds predictive models into multidisciplinary teams spanning DMPK, toxicology and safety pharmacology, and prototypes LLM-driven agent workflows for design-make-test-analyse cycles.

ChemAxon · RDKit · Pipeline Pilot +2

• 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

• USA - Pennsylvania - Upper Providence
• US$139,425 – US$232,375 pa
• Director

Acts as the operational hub for oncology assets, owning the integrated project plan, budget and risk inputs while driving critical-path acceleration and governance decisions. Partners with project leads to navigate uncertainty, facilitate high-performing teams and embed consistent project management practices across the pipeline.

Planisware · MS Project

• Waltham, United States
• US$139,425 – US$232,375 pa
• Director

Acts as the operational 'COO' of a drug or vaccine asset, owning the single integrated project plan and partnering with project leads to steer strategy through complexity. Drives critical-path acceleration, risk management, governance preparation and cross-functional handoffs, with budget and resource forecasting using tools such as Planisware or MS Project.

Planisware · MS Project

• UK - Hertfordshire - Ware RD
• Director

Provides scientific and medical expertise at study level across early- and late-phase hepatology assets, leading protocol and study document development, serving as medical monitor for Phase 1–4 trials, and interpreting efficacy, safety and biomarker data. Works within cross-functional global study teams and the Clinical Matrix Team, with informal coaching of less experienced clinical scientists and no formal line management.

• London
• Director

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents the Safety Evaluation & Risk Management function on cross-functional clinical matrix and project teams, escalating emerging safety issues to senior governance. Mentors junior staff and partners with Safety Physicians to shape long-term safety strategy.

• Poznan Grunwaldzka
• PLN 525,750 – PLN 876,250 pa
• Director

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix environment.

• Belgium-Wavre
• €141,000 – €235,000 pa
• Director

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix.

• Siena, Italy
• €124,500 – €207,500 pa
• Director

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix environment.

• Stevenage
• Hybrid
• Director

Provide strategic statistical leadership for global medical affairs and market access across GSK's oncology portfolio, designing and analysing non-registrational studies, secondary publications and ISR reviews. Partner with R&D, medical, commercial, RWE and Health Outcomes teams on HTA and payer evidence, using R, Python or SAS to develop novel statistical methods.

R · Python · SAS

• Cambridge
• Hybrid
• US$232,650 – US$387,750 pa
• Director · manages people

Leads CMC's scientific data, application and agentic AI product portfolio, setting integrated strategy and roadmap across forward-deployed engineering, product management and AI product strategy. Accountable for delivery quality, GxP compliance, governance, budget and headcount, and for representing the capability to R&D, Global Supply Chain, Quality and enterprise leadership.

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

Sits within GSK's Chemical Manufacturing & Control function, identifying and sizing AI opportunities across process development science for oligonucleotides, ADCs and monoclonal antibodies. Partners with forward deployed engineering pods to turn ambiguous business problems into scoped, buildable products, and shapes self-driving lab and in silico modelling initiatives.

Self-Driving Labs · Agentic Workflows · Physical AI

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

Sits within GSK's Chemical Manufacturing & Control function, shaping how AI transforms manufacturing sites worldwide. Runs day-to-day tech transfer engagement with sites and CMOs, sizes AI opportunities, defines target process, data and agent architecture, and drives agentification and recipe building for new products alongside forward deployed engineering pods.

MES · LIMS · ERP +6

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

Sits within GSK's Chemical Manufacturing & Control function, running day-to-day tech transfer engagement with manufacturing sites and CMOs while redesigning processes in detail. Shapes NPI launch strategy covering site impact assessment, capacity management, digital twins, scenario planning and virtual line commissioning, and defines the target process, data and agent architecture. Owns the tech transfer package and drives agentification and MES-ready recipe building alongside forward deployed engineering pods.

MES · LIMS · ERP +6