Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• On-site
• US$242,550 – US$404,250 pa
• Director · manages people

Senior physician leader providing medical oversight, safety monitoring and clinical insight across lung cancer studies, from protocol design through data interpretation. Serves on the Clinical Matrix Team, contributes to regulatory interactions and external scientific engagement, and mentors Medical Directors within the programme. Requires deep lung cancer drug development expertise, including early phase trials.

• Warsaw, Poland
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development of GU oncology assets, designing and executing Phase 1-3 trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds external expert relationships and contributes to business development diligence.

Real World Evidence (RWE)

• Livingston
• Mid-level

Leads strategic sourcing of animal models, especially rodents and genetically engineered strains, for an early-phase discovery business. Manages supplier relationships, RFIs/RFPs, contract negotiations and performance reviews, while partnering with scientific, veterinary and quality teams on capacity planning, welfare and regulatory compliance.

• London
• Remote
• Freelance

Supports UK clinical trial start-up by collecting and reviewing site and regulatory documentation, preparing submission packages, and coordinating Informed Consent Form adaptations. Liaises with investigative sites and internal study teams to resolve outstanding documents and track progress against milestones, ensuring ICH-GCP and local regulatory compliance.

• Harrow
• Remote
• Senior

Acts as principal labelling strategist within Global Regulatory Affairs, driving development and maintenance of dCCDS, CCDS, USPI and EU SmPC documents across an assigned product portfolio. Leads Global Labeling Committee reviews of proposed label exceptions and represents labelling on regulatory strategy teams, working with safety, clinical and commercial stakeholders. Home or office based across European locations.

Company Core Data Sheet (CCDS) · Development Company Core Data Sheet (dCCDS) · US Prescribing Information (USPI) +3

• Lisburn
• On-site
• Entry level
• Internship

A 12–14 month university placement for penultimate-year students, supporting the Statistical Programming group on clinical trials. Day to day you produce analysis and submission datasets, statistical tables, graphs and data listings using SAS, while learning about the pharmaceutical industry, clinical trial conduct and good clinical practice within a global project team.

SAS · R · MATLAB +1

• Maidenhead
• Senior

Leads safety surveillance and signal detection across a product's lifecycle, reviewing clinical and post-marketing data and contributing to aggregate safety reports and risk management plans. Partners with Global Safety Leads and cross-functional teams, mentors junior scientists, and supports regulatory responses.

Microsoft Excel

• Maidenhead
• Hybrid · 3 days in office
• Director

Leads strategic sourcing and evaluation of external innovation opportunities in Haematology, identifying preclinical to Phase 1 assets and shaping early partnering strategies. Sits on the Therapeutic Area Leadership Team, co-leads New Product Opportunity reviews, drives cross-functional due diligence and works with Business Development on deal execution. Hybrid, three days a week at an R&D hub site.

• London
• Hybrid
• £47,540 – £88,289 pa
• Mid-level

Manage regulatory activities for clinical trial applications across an assigned portfolio, working with study teams, country leads and cross-functional partners. Anticipate regulatory risks, coordinate responses to Health Authority queries and maintain product information in compliance systems, while contributing to automation and simplification initiatives.

• London
• Hybrid
• £56,511 – £104,949 pa
• Mid-level

Lead the development and maintenance of global labelling documents for neuroscience medicines, translating clinical and safety data into compliant product information. Facilitate cross-functional discussions, support Health Authority responses, and ensure timely implementation of labelling changes across global and major markets.

• Stevenage
• Hybrid
• Director · manages people

Accountable for onboarding and ongoing performance management of apheresis and treatment centres supporting clinical and commercial CAR T-cell therapies across the UK and Rest of World. Serves as the technical operations single point of contact, conducting site assessments, training centre staff, supporting quality systems and deviations, and managing process change rollouts. Involves up to 50% travel and possible management of contract employees.

Electronic Data Management Systems

• Stevenage
• On-site
• Entry level

Support GMP compliance in a multi-product cell and gene therapy facility, reviewing batch manufacturing and QC records, managing controlled documentation, and preparing patient-specific labels. Work with cross-functional teams on batch release, quality events and inspection readiness, on a Sunday–Wednesday shift pattern.

• Cambridge
• Hybrid · 3 days in office
• Director

Leads three mandates for an infectious disease portfolio: defining end-to-end publication strategy from target selection to clinical development, securing grants and partnerships with NGOs and philanthropic funders, and horizon-scanning emerging biotechnology. Partners with discovery, clinical, data and external academic stakeholders, coaching teams and influencing senior decision-makers.

• Uxbridge
• Hybrid
• Senior

As a senior individual contributor in the Global Biometrics & Data Sciences function, you write and validate SAS programs to produce derived analysis datasets and clinical Tables, Figures and Listings, and contribute to electronic submission packages such as NDA, BLA and MAA. You also review Statistical Analysis Plans and Data Presentation Plans, partner with external vendors on programming standards, and independently lead programming assignments across multiple projects.

SAS · Pinnacle 21 · MS Office +3

• Church Stretton
• Senior

Technical lead role driving innovation in polymeric and silica particle technologies for chromatography, diagnostics and biopharma consumables. Involves independently designing and executing complex polymer synthesis, particle manufacture and surface functionalization, plus technology transfer from lab-scale prototypes to full production. Acts as internal consultant and escalation point for critical materials issues, mentors scientists and shapes long-term technology strategy.