Latest Biotech Research Scientist Jobs

SERM Senior Scientific Director, Oncology

This role involves leading the safety evaluation and risk management of GSK's oncology assets in clinical development. Responsibilities include pharmacovigilance activities, safety data interpretation, and strategic risk mitigation. The position requires extensive experience in pharmacovigilance and a strong scientific background.

GSK Poznań, Powiat Poznań, Poland

SERM Senior Scientific Director, Oncology

This role involves leading the safety evaluation and risk management of oncology assets in clinical development at GSK. Responsibilities include pharmacovigilance activities, signal detection, and strategic safety planning, with a focus on ensuring robust benefit-risk profiles and patient protection.

GSK Wavre, Walloon Brabant, Belgium £141,000 – £235,000 pa

Associate Director, CMC Regulatory Science, International

This role involves leading CMC regulatory strategy for global mRNA product development, preparing and reviewing regulatory submissions, and guiding cross-functional teams on compliance and agency interactions. The position requires deep expertise in biologics CMC regulations, particularly in EU and ROW markets, and plays a key part in shaping regulatory pathways across vaccines, oncology, and rare diseases. Based at the Harwell site, it emphasizes in-office collaboration within a multidisciplinary team.

Moderna Clinical Development

On-site Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assays (LBA) in support of Moderna’s mRNA-LNP therapeutic programs. The Principal Scientist will oversee regulated bioanalytical activities including assay development, validation, and sample analysis, ensuring compliance with GcLP, GLP, and GCP standards. The position plays a key role in clinical development by generating high-quality data to inform regulatory submissions and advance innovative medicines, with opportunities to engage in AI-enabled and digital analytical approaches.

Moderna Clinical Development

Hybrid Permanent

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

Lead In Silico Business Partner, Platform

The Lead In Silico Business Partner, Platform role involves managing the relationship between Evotec's Drug Discovery Platforms and the In Silico & AI organization. Responsibilities include shaping the in silico and AI roadmap, translating scientific needs into requirements, and ensuring the delivery of high-quality in silico solutions across various platforms. The role also has a commercial mandate to drive adoption and value from in silico capabilities.

Evotec Abingdon, Oxfordshire, United Kingdom

SERM Senior Scientific Director, Oncology

This role involves leading the safety evaluation and risk management of GSK's oncology assets in clinical development. Responsibilities include pharmacovigilance activities, signal detection, and strategic safety issue evaluation, with a focus on ensuring robust benefit-risk profiles and patient protection.

GSK Siena, Province of Siena, Italy

SERM Medical Director

This role involves leading pharmacovigilance and risk management strategy for GSK’s global pharmaceutical assets, with a focus on patient safety across clinical development and post-marketing phases. The Medical Director will lead safety governance, drive signal detection and risk mitigation, and represent GSK in regulatory discussions. It requires deep expertise in drug safety, cross-functional leadership in a matrix environment, and strategic input into global safety operations.

GSK London, Greater London, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Science - UK

This role involves shaping and driving CMC regulatory strategies for UK-manufactured and UK-licensed mRNA products, from development through commercialisation and post-approval lifecycle management. You will work with cross-functional teams to ensure regulatory compliance, navigate MHRA requirements, and influence global regulatory decisions.

Moderna London, Greater London, United Kingdom

Associate Director, CMC Regulatory Science - UK

This role involves shaping and driving CMC regulatory strategies for UK-manufactured and UK-licensed mRNA products, from development through commercialisation and post-approval lifecycle management. You will work with cross-functional teams to ensure regulatory compliance and navigate complex MHRA requirements, contributing to global regulatory strategies and leading regulatory submissions.

Moderna Clinical Development

Associate Director, CMC Regulatory Science - UK

This role involves shaping and driving CMC regulatory strategies for mRNA products, from development through commercialisation and post-approval lifecycle management. You will work with cross-functional teams to ensure regulatory compliance and navigate complex MHRA requirements, while contributing to global regulatory strategies.

Moderna Didcot, Oxfordshire, United Kingdom