Latest Research Scientist Jobs

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development activities for GSK’s oncology portfolio, with a focus on genitourinary (GU) cancers. The Senior Medical Director will design and oversee phase 1–3 clinical trials, ensure scientific integrity, and collaborate with internal teams and external experts to advance drug development. The position plays a key role in regulatory submissions, lifecycle management, and shaping clinical strategy in a global, matrixed environment.

GSK Stevenage, United Kingdom US$284,250 – US$473,750 pa

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for genitourinary (GU) oncology programs within GSK’s pipeline, with responsibility for designing and executing phase 1–3 trials, ensuring scientific integrity, and supporting regulatory submissions. The Senior Medical Director will collaborate across functions and represent GSK externally with key experts and at medical meetings, driving data generation and strategic input for innovative oncology therapies.

GSK £284,250 – £473,750 pa

Hybrid Permanent

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves designing and deploying production-grade AI systems to enhance clinical development and operations at Pfizer. The director will lead the implementation of LLMs and agentic AI, building scalable, reproducible workflows that improve clinical trial processes such as protocol feasibility, site selection, and supply forecasting. They will collaborate closely with scientific and operational teams to translate complex needs into trusted, enterprise-scale AI solutions while championing MLOps and data governance best practices.

Pfizer United States US$176,600 – US$294,300 pa

On-site Permanent

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves leading the design and deployment of production-grade AI systems within Pfizer's Clinical Development & Operations organization. The Director will focus on applying LLMs and agentic AI to real-world clinical workflows, building scalable MLOps pipelines, and translating complex data into decision-support tools. They will collaborate closely with scientists and digital teams to drive trusted, enterprise-wide AI adoption in a regulated environment.

Pfizer London, SW7 2AP, United Kingdom US$176,600 – US$294,300 pa

Hybrid Permanent

Bioinformatics Engineer, London

This role involves building and maintaining a high-fidelity biological data layer to support machine learning at Isomorphic Labs. You will develop large-scale bioinformatics pipelines, harmonize public and internal datasets, and collaborate with cross-functional teams to ensure data quality and standardization. Your work will directly accelerate drug discovery by providing robust, integrated biological data for AI-driven research.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Software Engineer (Inference Platform), London

This role involves developing and operating a high-performance inference platform to serve large-scale machine learning models for drug discovery. You'll work closely with research and applied ML teams to scale and harden AI systems, focusing on reliability, throughput, and infrastructure stability. The position requires expertise in distributed systems, Kubernetes, and cloud-native ML deployment.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Director, Evidence Generation

This role involves leading the scientific oversight of global evidence generation studies, from Phase IIIb/IV trials to real-world evidence programmes. You will develop and implement integrated evidence strategies, influence product medical strategy, and engage with global stakeholders, including key opinion leaders and patient organisations.

Novartis London, United Kingdom

Hybrid Permanent

Associate Director, Translational Medicine Expert, TM Clinical Pharmacology

This role involves leading and managing multiple First-in-Human and Clinical Pharmacology studies, ensuring medical and scientific excellence. You will provide expert input into study design, safety, and reporting, and collaborate with cross-functional teams to align on program objectives and optimize processes.

Novartis London, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves providing hands-on IT support for Moderna’s GMP manufacturing operations at the Harwell site. Key responsibilities include ensuring GMP compliance, triaging IT incidents, managing infrastructure, and collaborating with various teams to maintain robust and compliant systems. The position offers exposure to modern observability and cybersecurity tools, making it a dynamic opportunity for someone who thrives in complex, regulated environments.

Moderna Oxford, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves supporting Moderna’s manufacturing operations at the Harwell site, ensuring GMP compliance and providing Tier 1 IT support. Responsibilities include maintaining robust IT systems, triaging incidents, managing infrastructure, and collaborating with various teams to ensure smooth operations. The position offers exposure to modern cybersecurity and automation tools, making it a dynamic and challenging opportunity in the biotech industry.

Moderna

On-site Permanent

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 mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Director, Global Product Lead, Early Oncology R&D

This role involves leading global product teams in early oncology R&D, from candidate selection through Phase III investment decisions. Responsibilities include shaping development strategies, engaging stakeholders, and ensuring ethical standards in oncology research.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, defining statistical strategies, ensuring appropriate methodologies, and collaborating with cross-functional teams. They also manage outsourcing operations, represent Biostatistics in regulatory interactions, and support innovation in clinical trial design and analysis.

CSL

On-site Permanent

Associate Director, Biostatistics (4)

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...

CSL

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