Biotechnology Jobs

• Zebulon, United States
• US$202,125 – US$336,875 pa
• Director

Drives the development and execution of the analytical/QC testing network strategy across the global supply chain, translating approved strategy into an operational roadmap and securing endorsement from governance forums such as the Supply Chain Review Board. Partners with GSC Quality, MSAT and R&D on NPI and commercial supply, benchmarks industry best practice, and builds KPI reporting for senior leadership. Focuses on analytical testing strategy for large molecules, ADCs and Oligos.

• Upper Merion
• US$202,125 – US$336,875 pa
• Director

Drives the development and execution of the analytical network strategy across GSK's supply chain, defining QC testing network principles and translating them into an operational roadmap. Collaborates with GSC Quality, MSAT and R&D, benchmarks industry best practice, and establishes KPIs and reporting for senior leadership. Focuses on analytical testing strategy for large molecules, ADCs and Oligos.

• Oxford
• Remote
• £60,000 – £80,000 pa

Serve as the primary scientific resource for customers after instrument installation, guiding onboarding, training and advanced fluorescence imaging workflows. Troubleshoot sample preparation, image acquisition and data analysis issues, build training materials, and feed customer insights to product teams. Remote-based with around 25% travel across the UK and Europe for installations.

• Oxford
• On-site
• £40,000 pa
• Senior
• Permanent

Develops and optimises LC-MS workflows for low-input and single-cell proteomics and/or metabolomics, supporting researchers across the institute with experiment design, method development, data acquisition and interpretation. Works closely with bioinformatics, scientific computing and AI/ML teams, and helps build SOPs and training material for single-cell MS capability.

LC-MS · Flow Cytometry · Sequencing +5

• Cambridge
• Hybrid · 3 days in office
• Director

Lead digital health strategy engagements with AstraZeneca R&D, top pharma and biotechs, shaping operating models and roadmaps across clinical development. Directs project teams on AI and digital solutions such as ePRO/eCOA, wearables and digital biomarkers, building business cases and tracking value realisation. Combines consulting, protocol design support and scaled implementation in a matrixed environment.

ePRO · eCOA · Wearables +1

• London
• Hybrid
• Senior
• Permanent

Acts as subject-matter expert for the organisation's ELN platform, owning its configuration, governance and continuous improvement across R&D laboratories. Builds workflows, templates and integrations, supports superusers, and leads development of a centralised Technical Development data repository using SQL and analytics to enable data-driven scientific decisions.

Benchling · JMP · APIs

• United Kingdom - Walton Oaks
• Hybrid

Lead and implement regional regulatory strategies for assigned products, acting as the regional representative within Pfizer's Global Regulatory Strategic Team. Accountable for timely submissions, approvals and optimal interactions with Health Authorities, partnering cross-functionally to align regulatory plans with commercial goals.

ChatGPT · Microsoft Copilot

• United Kingdom
• Remote
• Senior

Acts as independent Principal Investigator overseeing qualitative in-trial research studies, from design through delivery, for pharmaceutical clients. Applies methods like interviews and surveys to capture patient experience data, manages project budgets and timelines, and contributes to proposals and client development. Requires CAQDAS expertise and strong scientific writing.

Atlas.ti · NVivo · MAXQDA +1

• Harrow
• Hybrid
• Mid-level

Drives strategic impact by developing operational and technical solutions for Early Phase clinical trials, collaborating with Enterprise Accounts, Growth Accounts, Commercial Operations and Strategic Business Units. Contributes to business development from opportunity identification through solution design, bid strategy and client engagement, crafting differentiated value propositions and proposal content. Requires 3-5 years of Early Phase Clinical Trials experience and up to 30% travel.

Clinical Trial Management Systems · Proposal Development Platforms · Enterprise Software Solutions

• Reading
• Senior

Embedded with a global pharmaceutical sponsor, you own end-to-end clinical supply strategy across complex trials: protocol interpretation, label text, demand forecasting, packaging, IRT setup, distribution and temperature-excursion management. You lead vendor oversight, risk assessments and budget tracking while advising study teams and client leadership.

IRT · RTSM · ERP +3

• Madrid, Spain
• Hybrid
• Senior

Builds, trains, deploys and maintains AI/ML models and automation tools for supply chain master data within Pfizer's Supply Planning Data Intelligence group. Work spans optimization algorithms, predictive models, generative AI/NLP, and autonomous data agents integrated with planning systems like Kinaxis, owning solutions from development through production handover.

scikit-learn · pandas · TensorFlow +7

• London
• Remote
• Director

Provides statistical consulting and strategic advice on optimal study designs and analyses across drug, device, and diagnostic clinical development, including preparation for regulatory authority interactions. Serves as a leader in innovative study designs for client accounts and supports new business through proposals, bids, and client presentations, representing clients at key regulatory meetings.

FDA · EMEA · MHRA +2

• Cambridge
• Hybrid · 3 days in office
• Lead · manages people
• Permanent

Accountable to the Global Clinical Head for an indication-aligned cluster of late-phase Respiratory and Immunology studies, supervising Global Development Medical Directors and Scientist Directors. Leads cross-functional design, conduct, monitoring and data interpretation, represents the program at health authority interactions, and co-leads publication strategy.

• High Wycombe
• Entry level
• Internship

A 12-month industry placement within the Integrated Data Analytics and Reporting function, focused on Clinical and Statistical Programming. The student applies SAS, R, Python, RPA and Power Automate to analyse trial data, build AI-driven tools and automate clinical reporting, while collaborating with programming experts across disease areas.

SAS · R · Python +4

• Oxford
• Hybrid · 3–4 days in office
• Director

As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.

R · Phoenix WinNonlin · NONMEM +2