Biotechnology Jobs

• 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

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

Leads a team of risk and compliance business partners supporting GSK's R&D technology, covering clinical, discovery and regulatory systems. Combines hands-on cyber risk consulting and assurance with team leadership, owning the risk register, GxP/SOX compliance, audit readiness and stakeholder engagement across Ware and London sites.

ServiceNow

• Manchester
• Senior

Conducts site qualification, initiation, monitoring and close-out visits for a dedicated sponsor program, ensuring GCP compliance, patient safety and data integrity. Builds investigator relationships, resolves queries, mentors junior staff and supports recruitment and start-up activities, with up to 40-60% regional travel.

Investigator Site Files (ISF) · Trial Master Files (TMF)

• Bath
• Senior

As an embedded Senior CRA within IQVIA's Clinical Functional Service Partnership model, you conduct site qualification, initiation, monitoring and close-out visits while safeguarding patient safety, data integrity and protocol compliance. You mentor junior team members, manage site relationships and recruitment strategies, and travel up to 40-60% across the region.

Investigator Site Files · Trial Master Files

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

Execution-focused role supporting the President's executive suite, handling physical meeting preparation, guest hospitality, travel-day logistics and event setup. Coordinates with internal stakeholders and external workplace teams, travelling to offsites to manage room layouts and on-the-ground logistics. Reports to the President's Executive Assistant within a tight-knit support ecosystem.

• Cambridge, United States
• Hybrid · 3 days in office
• Lead

Lead DMPK strategy across drug discovery projects, designing screening cascades and mechanistic experiments while integrating DMPK, PD and toxicology data for dose and safety predictions. Work closely with AI/ML platform teams to optimise computational ADME models and author regulatory sections, in a hybrid Cambridge, MA role.

Python · R

• London
• Hybrid
• £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 role with remote option for UK candidates over 50 miles from the London office.

• Welwyn
• On-site
• Lead · manages people

Drives and facilitates efficient study start-up for Roche-sponsored clinical trials across the UK, developing start-up strategies and overseeing site activation and regulatory compliance. Engages with Ethics Boards, Health Authorities and CROs, manages budgets and contracts, and champions process automation and team development.

REC · MHRA · HRA

• 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.

• Cambridge
• Senior
• Permanent

Lead biophysical binding characterisation, predominantly using Surface Plasmon Resonance, to interrogate Bicycle® molecules and triage screening cascades. Design and optimise bespoke assays, explore orthogonal technologies such as Carterra, AlphaScreen and mass photometry, and partner with computational and structural biology teams on structure-based drug design. Mentors junior colleagues within the Platform Technology group.

SPR · Carterra · AlphaScreen +4

• 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

• London
• Hybrid
• £50,733 – £59,484 pa
• Mid-level
• Contract

Lead the harmonisation, integration and analysis of large-scale multi-omics datasets including single-cell transcriptomics, epigenomics and proteomics, building reproducible Nextflow or Snakemake pipelines on HPC or cloud infrastructure. Work with AI and mathematical modelling teams within a multidisciplinary consortium spanning Imperial, UCL and industry partners on an ARIA-funded programme studying innate immune protection against respiratory viral infections.

Nextflow · Snakemake · Unix +3

• Cambridge
• Hybrid · 3 days in office
• Senior

Lead UK direct tax compliance and group tax reporting for a FTSE 100 biopharmaceutical business, preparing and reviewing corporation tax computations, patent box and capital allowance claims, and quarterly and year-end tax provisions under Sarbanes-Oxley. Handle HMRC audit queries and negotiations, advise the UK business on legislation changes, and drive process efficiencies through automation and AI.

AI

• Luton
• Hybrid · 3 days in office
• Senior

Lead UK direct tax compliance and reporting for a FTSE 100 biopharmaceutical group, preparing and reviewing corporation tax computations, patent box and capital allowance claims, and quarterly and year-end tax provisions. Advise the UK business on legislation changes, HMRC audits and governance regimes, while driving process efficiencies through automation and AI.

• Wirral
• Hybrid
• Lead

You will act as the bridge between internal science teams and external CDMOs, reviewing batch records, assessing facility fit, troubleshooting manufacturing issues and presenting risk assessments to leadership. The role spans the full range of chemical engineering unit operations for small molecule and ADC scale-up, with up to 50% remote working and up to 20% international travel.