Discover Biotechnology job opportunities in Leeds

Spotlight

Senior Computational Chemist, LNP Design

This role involves leading the computational design of lipid nanoparticles for nucleic acid delivery, using chemical and biophysical principles, AI tools, and molecular simulations. You will work closely with the experimental team to translate computational insights into testable strategies and refine formulations iteratively.

CureAge Therapeutics London, Greater London, United Kingdom

Hybrid Permanent Part-time

Spotlight

Senior Clinical Trial Case Manager

This role involves leading safety data review and pharmacovigilance activities within clinical trials, ensuring compliance with international regulations such as GxP. The individual will mentor team members, manage CAPAs, support regulatory inspections, and contribute to safety reporting and risk management. Key responsibilities include MedDRA coding, safety data analysis, and developing pharmacovigilance procedures to support global regulatory requirements.

CSL Maidenhead, Berkshire, United Kingdom

On-site Permanent

Field Service Engineer - Leeds, Yorkshire, Manchester & Liverpool

This role involves providing electro-mechanical hardware support, troubleshooting, preventive maintenance, and installations for Roche Diagnostics' customers in the North of England. You will work closely with sales and service teams to ensure customer satisfaction and technical excellence.

Roche United Kingdom

Clinical Data Management Placement Year 2027 - Leeds

This 12-month placement year in Clinical Data Management at Fortrea involves hands-on experience in managing clinical trial data, working with state-of-the-art technology, and collaborating with a global team. Responsibilities include data entry, validation, and reconciliation, contributing to the development of life-changing treatments.

Fortrea Leeds, West Yorkshire, United Kingdom

On-site Internship

2027 University Student Placement - Clinical Research Technician

This 12-month placement offers hands-on experience in clinical operations and screening, working directly with patients and volunteers in Phase I clinical trials. You'll receive comprehensive training, mentorship, and exposure to real-world drug development processes.

Fortrea Leeds, West Yorkshire, United Kingdom

Clinical Monitoring Analyst (Cluepoints)

The Clinical Monitoring Analyst (CMA) role involves setting up, programming, and refreshing the Centralized Monitoring platform for clinical trials. Key responsibilities include developing the CM strategy, implementing Quality Tolerance Limits (QTL), Key Risk Indicators (KRI), and Data Quality Assessments, and maintaining the platform's specifications. The role requires strong SAS programming skills, experience in pharmaceutical R&D, and the ability to work autonomously and collaboratively.

IQVIA London, Greater London, United Kingdom

Remote

Head of Patient-Facing Quality Assurance

This role leads the global quality and compliance function for pharmacovigilance (PV) systems, ensuring adherence to international regulations and internal standards across clinical safety, regulatory affairs, and medical affairs. The position combines strategic oversight with hands-on operational leadership, including audit strategy, inspection readiness, deviation and CAPA management, and cross-functional GxP guidance. It requires deep technical expertise in PV processes and strong leadership to drive quality across global teams and third-party vendors.

CSL Maidenhead, Berkshire, United Kingdom

Senior Manager - Regulatory Project and Resource Management (HIV)

This role involves managing regulatory planning and resource management for GSK’s HIV medicines portfolio, including creating and maintaining Regulatory Development Plans, forecasting resources and costs, and supporting governance cycles. The position requires strong experience in regulatory project management, advanced knowledge of Planisware, and the ability to collaborate with cross-functional teams.

GSK London, Greater London, United Kingdom

Translational Medicine Expert – Gastroenterology, Associate Director

This role involves leading early-phase clinical development (Phase 1 and 2) of novel gastroenterology therapies, with a focus on inflammatory bowel disease (IBD). The Translational Medicine Expert will design clinical development plans, serve as medical lead for trials, and collaborate closely with research, biomarker, and late-phase development teams. The position requires strong scientific leadership, engagement with key opinion leaders, and active involvement in regulatory interactions.

Novartis London, Greater London, United Kingdom £67,900 – £126,100 pa

Director - Diagnostic Execution (Oncology Translational Medicine)

This role involves leading the operational delivery of biomarker and diagnostic strategies for GSK's oncology portfolio, particularly focusing on Antibody Drug Conjugate (ADC) development. Responsibilities include managing a team, overseeing external testing partners, and ensuring regulatory compliance and successful drug-diagnostic co-development.

GSK Stevenage, Hertfordshire, United Kingdom

Undergraduate Regulatory Strategist

This role involves working in Pfizer's Regulatory Strategy department, contributing to the development and implementation of regulatory strategies for innovative medicinal products. Responsibilities include compiling regulatory documents, engaging with health authorities, and maintaining systems and processes. The position offers a unique overview of the pharmaceutical product life cycle from research to market.

Pfizer United Kingdom - Walton Oaks

Clinical Supply Coordinator

The Clinical Supply Coordinator ensures timely delivery of clinical trial supplies, manages inventory, forecasts demand, and oversees packaging and distribution. They also maintain compliance, manage risks, and support client and vendor meetings.

IQVIA Manchester, Greater Manchester, United Kingdom

Director, Pharmacovigilance

Leads global pharmacovigilance and safety strategy for gene therapy products, overseeing signal management, risk assessment, and benefit-risk profiling across investigational and marketed phases. Provides medical oversight for clinical trials, including safety data review, SAE evaluation, and regulatory submissions. Collaborates cross-functionally to ensure compliance with global safety regulations and supports health authority interactions on product safety matters.

Orchard Therapeutics London, Greater London, United Kingdom

Hybrid Permanent

Supply Chain Industrial Placement (12 months)

This 12-month industrial placement involves working with the International Supply Chain team at Vertex Pharmaceuticals' London HQ. You'll gain hands-on experience in commercial supply operations, ensuring medicines reach patients globally. The role offers a hybrid or on-site work pattern and emphasizes learning from industry experts.

Vertex Pharmaceuticals London, Greater London, United Kingdom

Hybrid Internship

VP Head of AI

The VP Head of AI leads Evotec's AI Accelerator, responsible for developing predictive models, AI-generated hypotheses, and agentic workflows to enhance drug discovery. The role involves setting the AI vision, managing the AI stack, and building a team of senior AI talent.

Evotec Abingdon, Oxfordshire, United Kingdom

Commercial Haematology Industrial Placement (12 Months)

This 12-month industrial placement with Vertex Pharmaceuticals' International Haematology team involves hands-on experience in commercialising a gene therapy product. You will work closely with industry experts, gain insights into the biotech/pharmaceutical industry, and contribute to launch strategies and activities.