Biotechnology Jobs

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating these into clinical plans to optimize decision-making and patient stratification.

GSK £189,750 – £316,250 pa

On-site Permanent

Interventional Study Scientist Director

This role involves leading the scientific design and execution of interventional clinical studies in oncology or hematology, ensuring high standards of quality and ethics. You will collaborate with cross-functional teams, provide scientific oversight, and engage with healthcare professionals to deliver impactful results.

GSK

On-site Permanent

GMP Vendor Oversight and QA Lead

This role involves leading the quality oversight of external partners in R&D and regulated activities, ensuring compliance with GxP standards. Responsibilities include vendor lifecycle management, risk-based monitoring, quality agreements, and cross-functional collaboration to maintain high-quality standards and continuous improvement.

CSL United Kingdom

On-site Permanent

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role involves leading the quality oversight of external partners in R&D and regulated activities, managing the vendor lifecycle from due diligence to continuous improvement, and ensuring compliance with GLP/GCP/GMP/GVP standards. The position requires close collaboration with various departments to maintain high-quality standards and regulatory compliance.

CSL United Kingdom

On-site Permanent

Director – Process Design and Optimisation in Chemical Development

This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Senior Scientist – 12-month - Pharmaceutical Sciences

This role involves developing analytical control strategies and methodologies to support the manufacturing of clinical active pharmaceutical ingredients (APIs) for both small molecules and novel modalities like oligonucleotides and peptides. The scientist will work within the Early Chemical Development (ECD) group, collaborating with chemists and external partners to interpret complex data, improve processes, and ensure compliance with GMP and safety standards. The position emphasizes innovation, scientific rigor, and the application of advanced technologies including AI and automation.

AstraZeneca Macclesfield, United Kingdom

On-site Contract

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays such as RT-qPCR, dPCR, and NGS to support clinical biomarker strategies across Moderna’s therapeutic pipeline. The scientist will work hands-on in assay design, optimization, and data interpretation, ensuring compliance with GCLP standards while integrating genomics, bioinformatics, and clinical insights. Collaboration with cross-functional teams is key to translating molecular data into actionable decisions for drug development.

Moderna Oxford, United Kingdom

Hybrid Permanent

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves leading high-parameter spectral flow cytometry activities in a GCLP-compliant clinical laboratory, generating immunophenotyping and functional immune profiling data from PBMC and whole blood samples to support mRNA-based clinical development. The scientist will independently execute and analyze complex assays, contribute to assay development and validation, and ensure regulatory compliance while leveraging advanced platforms like the Cytek Aurora. Opportunities exist to engage with digital tools and generative AI for data interpretation and workflow optimization within a collaborative, innovation-driven environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Software Engineer (Training Platform)

You will play a key role in building and operating the inference platform, connecting deep expertise in distributed systems programming with hands-on knowledge of Kubernetes-based platforms. Your responsibilities will include developing and maintaining the platform, supporting users, and improving CI/CD processes, all while serving cutting-edge machine learning models for scientific applications.

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

Head of DMPK

The Head of DMPK will lead the strategic direction of drug metabolism and pharmacokinetics, ensuring robust scientific excellence and predictive modeling. Key responsibilities include defining DMPK strategies, collaborating with data science teams, and leading a high-performing team.

Recursion London, United Kingdom £166,500 – £208,100 pa

Hybrid Permanent

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs. Responsibilities include designing clinical studies, authoring regulatory documents, and collaborating with cross-functional teams to expedite drug development.

Recursion North Tyneside, NE29 8EP, United Kingdom US$212,900 – US$297,000 pa

Hybrid Permanent

Regulatory Transparency (Disclosures) Professional

In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent

Country Study Start-Up Team Leader (cSTL)

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche Welwyn Hatfield, United Kingdom

Medical Device Programme Lead

Balance technical, regulatory and commercial challenges in this fulfilling roleThis highly regraded Cambridge-based medical technologies company is seeking a proven engineering leader to help guide high-value development programmes from concept through to transfer to manufacture. Your leadership will accelerate development...

ECM Selection Cambridge, Cambridgeshire, United Kingdom £75,000 – £95,000 pa