Biotechnology Jobs

Clinical Data Analyst – Evinova

The Clinical Data Analyst role involves managing and optimizing clinical trial data, collaborating with cross-functional teams, and contributing to the development of data products. Responsibilities include data management, standards validation, pipeline configuration, troubleshooting, and continuous process improvement.

AstraZeneca London, United Kingdom

On-site Permanent

Executive Director, Strategy, Oncology R&D

This role involves owning and driving the global Oncology R&D strategy, setting priorities for the senior executive team, and transforming the approach to deliver impact for patients. You will craft integrated therapeutic area strategies, combining clinical, scientific, and commercial insights to shape portfolio choices and investment priorities.

AstraZeneca London, United Kingdom

On-site Permanent

Data Curator, London

As a Data Curator at Isomorphic Labs, you will work closely with AI experts and drug discovery scientists to curate high-quality, ML-ready datasets. Your role involves integrating large-scale biomedical and biochemical data, enhancing data quality, and collaborating across teams to build and improve data assets that fuel the company's mission to accelerate drug discovery using AI.

Isomorphic Labs London, United Kingdom

On-site Permanent

Data Scientist (Analytics), London

As a Data Scientist at Isomorphic Labs, you will work with a multidisciplinary team to analyze business intelligence data, implement telemetry, and design key metrics to optimize the drug design process. Your role involves providing actionable insights to drive decision-making across product, engineering, and research teams, and collaborating to build an analytics layer that supports efficient drug discovery.

Isomorphic Labs London, United Kingdom

On-site Permanent

Clinical Quality Assurance - Program Lead (Associate Director)

The Associate Director, Clinical Quality Assurance (QA) will lead quality oversight for clinical trials, ensuring compliance with health authority requirements and patient safety. Responsibilities include implementing quality strategies, monitoring risk management, and supporting governance for quality incidents. The role involves collaboration with key stakeholders and active participation in continuous improvement initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on ensuring compliance and timely approval of new and marketed products, serving as a regulatory liaison throughout the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Computational Protein Designer

Computational Protein DesignerThe opportunityWe are seeking a Computational Protein Design Scientist to join our team working at the interface of generative AI and synthetic biology. Working closely with our Lead Computational Protein Designer, you will play a key role amongst...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Member of Technical Staff - Reasoning Workflows

We are looking for a highly skilled Member of Technical Staff to lead the development of cutting-edge workflows. You will build autonomous systems that can navigate complex scientific tasks entirely through natural language conversation. In your role, you will architect...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Head of Engineering

This role involves leading and scaling the Engineering team, establishing strong engineering processes, and providing architectural oversight for a sophisticated AI-driven platform used by leading pharmaceutical companies. The position offers significant impact and ownership in a high-growth Series A business.

Harnham - Data and Analytics Recruitment London, United Kingdom £120,000 – £130,000 pa

Remote Permanent

Project Consultant

As a Project Consultant, you will manage client relationships and oversee the delivery of high-quality projects using Patient Cloud technology. Your responsibilities include managing study portfolios, leading cross-functional teams, and ensuring project milestones are met on time and within budget.

Randstad Engineering London, United Kingdom

Senior Product Manager

This role involves shaping the product strategy and roadmap for an AI-driven platform used in pharmaceutical research. You will work closely with engineering, commercial, and customer-facing teams to ensure the product delivers real-world value, while mentoring other product managers and supporting the company's growth.

Harnham - Data and Analytics Recruitment London, United Kingdom £90,000 – £105,000 pa

Remote Permanent

Laboratory Customer Service Role

This role involves providing high-quality customer support to patients and healthcare professionals, handling both simple and complex enquiries via phone and electronic channels. You will work in a fast-paced environment, managing administration tasks and ensuring each interaction reflects excellent customer service standards. The position is hybrid, with shifts in the office and from home, including weekends and bank holidays.

Ritz Recruitment Euston, London, NW1 2EA, United Kingdom £28,808 pa

Hybrid Permanent

SME - MSAT EM Technical Operations DS/DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The role also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Senior SME - MSAT EM Tech Ops DS DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, providing lifecycle support, and ensuring compliance with GMP standards. The role also focuses on continuous improvement and managing technical transfers between contract manufacturing organizations (CMOs).

GSK East Hertfordshire, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and supporting cross-functional teams in navigating international regulations.

Recursion London, W1C 2QP, United Kingdom £88,200 – £111,100 pa

Hybrid Permanent Flexible