Latest Research Jobs

Director, Global Strategic Insights – Oncology

This role involves leading the generation of strategic insights to shape the global product strategy for a key oncology brand in GSK's ADC portfolio. Responsibilities include driving commercial forecasts, conducting market research, and collaborating with cross-functional teams to ensure insights are integrated into business decisions and investment planning.

GSK United States

On-site Permanent

Director, Global Strategic Insights – Oncology

This role involves leading the generation of strategic insights for a key oncology brand within GSK's ADC portfolio. Responsibilities include shaping commercial forecasts, conducting global market research, and partnering with cross-functional teams to drive business strategy and competitive intelligence.

GSK

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory approvals and strategic insights.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This role involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The GDL also provides expert input on trial design, regulatory activities, and external stakeholder engagement.

Pfizer

On-site Permanent

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

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

Lead Software Engineer (Inference Platform), London

As a Senior or Principal Software Engineer, you will lead the development of a robust and scalable ML platform to support groundbreaking AI in drug discovery. Your responsibilities include architecting reliable infrastructure, optimizing inference services, and improving CI/CD processes to accelerate research and development.

Isomorphic Labs London, United Kingdom

On-site Permanent

Associate Director, Biostatistics

This role leads the statistical strategy and execution for clinical development programs within a therapeutic area, ensuring robust study design, data analysis, and regulatory compliance. The Associate Director collaborates with cross-functional teams, represents biostatistics in regulatory interactions, and oversees internal or outsourced programming efforts. They also drive innovation in statistical methodologies and contribute to clinical trial interpretation and reporting.

CSL

Hybrid Permanent

Environmental Risk Assessment Scientist - 6-month Secondment

This role involves preparing and maintaining Environmental Risk Assessments, monitoring outsourced environmental studies, and engaging with cross-functional teams on sustainability initiatives. The position offers hands-on experience in regulatory science and environmental data interpretation, with full training and mentoring provided.

AstraZeneca Macclesfield, United Kingdom

Hybrid Contract Flexible

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regional and global regulatory leads, partnering with directors on innovative regulatory strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca

On-site Permanent

Machine Learning Scientist - Quantum Chemistry

This role involves developing machine learning models grounded in quantum chemistry to accelerate small-molecule drug discovery. The scientist will create physics-informed algorithms to predict molecular properties and interactions, using proprietary datasets and high-performance computing. Collaboration with computational and experimental teams ensures direct application of models in real-world drug design workflows.

Roche

Hybrid Permanent

Machine Learning Scientist - Small Molecule Drug Design

Develop and apply machine learning models for small-molecule drug design with a focus on protein–ligand interactions, binding affinity, and molecular properties. Collaborate with computational chemists, structural biologists, and medicinal chemists to validate and refine ML-generated hypotheses. Work within a multidisciplinary team to drive innovation in drug discovery using structure-driven approaches and foundation models.

Roche Switzerland

Hybrid 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 collaborating with cross-functional teams to ensure compliance with US, EU, and ROW regulations.

Recursion United Kingdom £176,400 – £228,250 pa

Hybrid Permanent Flexible

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA submissions, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna Poland

On-site Permanent

Associate Director, Regulatory Affairs

This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent