Latest Drug Discovery Jobs

Senior Software Engineer (Inference Platform), London

This role involves leading the reliability and scalability of AI/ML infrastructure for biotech applications, focusing on GPU/TPU systems, workload orchestration, and inference services. The engineer will overhaul monitoring, improve CI/CD stability, and ensure robust platform performance to support cutting-edge drug discovery research. Close collaboration with research and applied ML teams is central to the role.

Isomorphic Labs London, United Kingdom

On-site Permanent

Software Engineer (TechOps), London

This role involves building and managing cloud infrastructure and DevOps tooling to support AI-driven drug discovery. You'll work across research, development, and production environments using GCP, Kubernetes, and Infrastructure as Code, collaborating closely with scientists, ML researchers, and engineers. The focus is on creating scalable, secure, and automated systems that accelerate scientific innovation in a fast-moving, interdisciplinary environment.

Isomorphic Labs United Kingdom

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, guides cross-functional teams, and represents the programme in regulatory and scientific forums. Based on-site with a future relocation to Cambridge, UK, the position emphasizes strategic clinical leadership within a global biopharma environment.

GSK

On-site Permanent

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, contributes to regulatory engagements, and mentors medical teams within a cross-functional environment. The position integrates physician expertise into clinical strategy and external scientific forums, focusing on advancing care in high unmet need cancers.

GSK

On-site Permanent

Director, Generative AI – Chemical Development

Leads the strategy and implementation of Generative AI and agentic workflows in chemical development to accelerate CMC processes and scientific decision-making. Drives adoption of AI in regulated environments, focusing on use cases like knowledge mining, report generation, and experiment planning. Works across scientific, compliance, and digital teams to embed responsible, scalable AI into routine workflows.

AstraZeneca Macclesfield, United Kingdom

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading and executing phase-appropriate bioanalytical strategies for immunogenicity and ligand binding assays (LBA) within Moderna’s mRNA-LNP therapeutic pipeline. The Principal Scientist will oversee assay development, validation, and sample analysis, ensuring regulatory compliance and scientific rigor across clinical programs. The position emphasizes collaboration with cross-functional teams, integration of emerging technologies including AI-enabled tools, and contribution to regulatory submissions and data interpretation in a GcLP-compliant environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Project Specialist, Clinical Supplies

This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapeutic trials, including coordination of labeling, packaging, distribution, and temperature-controlled logistics. The specialist ensures investigational products are delivered on time and compliantly to clinical sites, supports IRT system testing, monitors vendor performance, and drives digital innovation and process improvements in supply chain execution.

Moderna

Hybrid Permanent

Associate Director, Regulatory Diagnostics

This role involves designing and delivering global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, within drug development programs. The individual will lead regulatory submissions across the lifecycle, engage with health authorities, and ensure compliance with global regulations. Collaboration with cross-functional teams and external partners is central to advancing regulatory plans for innovative diagnostics in a hybrid working environment.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Medical Safety Lead - CRM

The role involves monitoring clinical safety data, conducting medical assessments of adverse events, and identifying safety signals using both individual and aggregate data. The Medical Safety Lead will apply AI-enabled tools to enhance pharmacovigilance processes and provide critical medical input into regulatory submissions and safety documentation. Collaboration with global cross-functional teams is central to integrating safety insights across drug development programs.

Novartis London, United Kingdom £67,900 – £126,100 pa

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

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent

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

Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.

Pfizer England

On-site Permanent