Biotechnology Jobs

• London
• US$188,100 – US$313,500 pa
• Director

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Sits in the Clinical Pharmacology and Quantitative Medicine organisation, partnering with digital medicine, translational imaging, modelling and data science teams, and drafting regulatory content for FDA, EMA and ICH submissions.

MIDD · QSP · AI/ML

• Stevenage
• US$188,100 – US$313,500 pa
• Director

Lead end-to-end application of Model-Informed Drug Development across the drug development lifecycle, from first-in-human studies through filing and lifecycle management, providing clinical pharmacology strategy and evidence generation. Draft and review regulatory content for FDA, EMA, CDE, PMDA and ICH, and build cross-functional partnerships across digital medicine, translational imaging, AI/ML and biostatistics. The role sits in the newly established Clinical Pharmacology and Quantitative Medicine organisation, reporting into the Respiratory, Immunology & Inflammation Research Unit.

MIDD · QSP · AI/ML

• Home Worker
• Remote
• £67,900 – £126,100 pa
• Lead · manages people

Lead and develop a global regulatory team delivering clinical trial submissions and approvals, combining people leadership with regulatory expertise. Drive process improvement, simplification and automation while building stakeholder partnerships across Regulatory Affairs. Hybrid or remote working within the UK, with occasional office presence in London.

• Field Force (England / Wales)
• Hybrid
• £32,690 – £60,710 pa

Site-facing role managing Phase I–IV clinical trial sites, acting as the primary contact between the sponsor and sites. Responsibilities include site initiation visits, training, on-site and remote monitoring, risk assessment and mitigation, and closeout activities, working closely with cross-functional teams to ensure data integrity and compliance.

• London
• Hybrid · 3 days in office
• Mid-level

Join a newly formed Scheduling team to own and extend systems orchestrating compute allocation for complex ML workloads on Kubernetes. You'll design scheduling policies like gang scheduling and topology-aware placement, build custom Kubernetes controllers and CRDs, and optimize GPU/TPU utilization while partnering with ML researchers on reliability and SLOs.

Kubernetes · Kueue · Volcano +4

• London
• Hybrid · 3 days in office
• Senior

Lead translational pharmacology for an AI-first drug discovery team, shaping neurodegeneration strategy and target validation. Bridge dry-lab predictive models with experimental biology, designing screening cascades and profiling AI-designed molecules. Manage CRO partnerships and serve as scientific lead for portfolio programs.

SPR · TR-FRET · Mass Spectrometry

• Reading
• Mid-level · manages people

Leads end-to-end delivery of regional and global clinical trials embedded within a sponsor's team, managing timelines, budgets, risk and cross-functional groups. Also supports bid defence presentations, vendor management and financial forecasting, mentoring less experienced project team members.

IQVIA

• Fordham
• On-site
• Senior
• Permanent

Hands-on role independently developing, optimising and validating analytical methods using LC-MS, troubleshooting complex analytical challenges and building new testing solutions for specialist laboratories. You own method development projects from feasibility through validation and implementation, working across the business in a busy commercial testing environment under ISO 17025.

LC-MS · GC-MS/MS · HRAM

• Manchester

Field-based role selling laboratory reagents and custom/bulk chemicals directly to customers and through top-tier distributors across Northern UK. You build territory plans, forecast, maintain CRM, train sales reps, and support trade shows, working with clients in pharma, food and beverage, and environmental testing. Requires a chemistry background and frequent travel.

CRM

• Abingdon
• On-site
• Entry level
• Permanent · Shift work

Operate pilot plant reactors and ancillary equipment in a GMP-regulated large-scale chemical production environment, running multiple syntheses, some never previously scaled. Duties include routine maintenance and reconfiguration of reaction vessels, environmental monitoring, accurate batch documentation, and shift handovers. The role follows a rotating 12-hour day and night shift pattern averaging 42 hours per week.

Microsoft Office

• High Wycombe
• Hybrid · 3 days in office
• Entry level
• Internship

A 12-week summer internship in EMEA Global Regulatory Affairs within the Oncology therapeutic area, working on a hybrid model with three days on site. Interns join a global matrixed team supporting clinical strategies and Phase I-III oncology studies, contributing to regulatory strategy, clinical trial applications and product registration activities, with a mentor, cross-functional team meetings and a research poster presented at a company-wide symposium.

Microsoft Outlook · Microsoft Excel · Microsoft PowerPoint +5

• Uxbridge
• Hybrid
• Director

Leads EU regulatory strategy for an immunology and cardiovascular portfolio, from early development through registration and lifecycle management. Acts as the regulatory lead for assigned development teams, negotiating with the EMA and other health authorities and building integrated submission plans. Integrates scientific, medical, legal and business perspectives while monitoring European regulatory trends.

EMA

• London
• Hybrid · 3 days in office
• Mid-level

Hands-on health economics role leading the delivery of cost-utility and budget impact models in Excel and VBA for national HTA submissions to NICE, SMC and AWMSG. Partners with UK Market Access, Medical and Brand teams plus the global HEOR function, and also builds early cost-effectiveness models for future brands and indications.

Microsoft Excel · Microsoft VBA

• Cambridge
• Senior

Design and develop novel mechatronic systems for medical devices, including liquid handling machines and surgical robotic systems, within a multidisciplinary R&D team. Take concepts through iterations to manufacture, designing intricate mechanisms while owning wider system development. Open on sector background, but complex mechatronics experience is key.

SolidWorks · Pro/ENGINEER

• London
• Remote
• Mid-level

Oversees medical coding activities across clinical studies, managing coding dictionaries such as MedDRA and WHODrug, reviewing coded data for accuracy and compliance, and preparing coding reports for medical review. Acts as subject matter expert, delivering training and partnering with Clinical Development, Pharmacovigilance and Data Management teams to drive process improvements and regulatory compliance.

MedDRA · WHODrug