Biotechnology Jobs

• London
• Senior

Leads complex global and multi-regional clinical trials from start-up through close-out, with accountability for quality, timelines, budgets, regulatory compliance and sponsor objectives. Acts as primary strategic partner to sponsors and directs cross-functional teams across regions, with a focus on renal, obesity and MASH studies.

• Liverpool
• Director · manages people

Leads the Operational Excellence function at a major influenza vaccine manufacturing site, deploying Lean, Six Sigma and the CSL Operating System to translate strategy into operational priorities and financial benefits. Owns the site management system, structured problem solving and continuous improvement, coaching senior leaders and leading the OE team. Reports to the Manufacturing Site Lead and sits on the Site Leadership Team.

CSL Operating System

• Barnard Castle
• On-site
• Shift work

Carries out planned preventative maintenance, fault finding and repairs on manufacturing, packaging and utility equipment in a sterile pharmaceutical plant, responding to breakdowns to minimise downtime. Works within a shift-based cross-functional team, using SAP CMMS and GMP documentation, and supports root cause investigations, CAPAs and continuous improvement.

SAP · CMMS

• 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.

• Philadelphia, United States
• US$203,775 – US$339,625 pa
• Director

Provides scientific and strategic leadership for real-world evidence supporting an mRNA vaccine portfolio, with a primary focus on influenza. Shapes evidence generation across late-stage development, launch and post-marketing, leading US post-marketing vaccine effectiveness studies and external academic and data-partner collaborations. Requires deep expertise in influenza epidemiology, real-world data and causal methods, plus influence across a global matrix.

Medicare · EHR

• London
• Hybrid · 3 days in office
• Lead

Drive DMPK strategy across drug discovery projects, designing screening cascades and mechanistic experiments while integrating AI/ML and PBPK modelling to predict human dosing, efficacy and safety windows. Work within an interdisciplinary team of drug design and machine learning specialists, authoring regulatory documents and optimising molecule design with chemistry leads.

R · Python · KNIME

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

Lead end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory and global distribution for an AI-first drug discovery company. Act as the clinical supply authority within a lean Pharmaceutical Sciences & CMC team, building scalable systems and vendor networks while partnering closely with Clinical Operations and CROs.

IRT · RTSM

• London
• Remote
• Lead

Supports the Centralized Monitoring Lead in building study-specific monitoring strategies, programming quality tolerance limits, key risk indicators and data visualisations on the Cluepoints platform. Handles platform setup, scheduled refreshes, specification documents and peer reviews, working directly with a sponsor on a dedicated project. Requires strong SAS macro skills and prior data management experience.

Cluepoints · SAS · EDC Systems +1

• Uxbridge
• Hybrid
• Director

As a member of cross-functional development teams, you will contribute to trial design, protocol development, analysis planning, and regulatory submissions, with the option to support a specific asset indication. The role involves authoring statistical analysis plans and clinical study reports, defending protocols at governance reviews, and providing statistical leadership on health authority requests. It requires 50% onsite presence in Uxbridge and proficiency in SAS, R, or Python.

SAS · R · Python

• 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.

• 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

• Cambridge
• £71,200 – £113,200 pa
• Senior · manages people

Leads day-to-day operations of a genomics hub, managing NGS workflows such as RNAseq, ATACseq and single cell genomics, plus SOPs, data management, equipment and budgets. Provides hands-on wet lab guidance and acts as subject matter expert on experimental design while training and supervising technical staff.

• Leeds
• Entry level
• Internship

A 12-month student placement in the clinical research department, supporting international trials of medical technology products. Duties include administering and coordinating the logistical aspects of clinical studies, tracking essential documents, and collecting and recording study data, with meetings alongside cross-functional partners.

Microsoft Excel · Microsoft Word · Microsoft PowerPoint