Latest Research Scientist Jobs

Regional EM Engineering Lead

This role involves ensuring strong engineering performance at Contract Manufacturing Organization (CMO) sites, focusing on Large Molecule Drug Substance. Responsibilities include site assessments, capital project management, and engineering support for new product introductions and existing GSK products.

GSK United States

On-site Permanent

Regional EM Engineering Lead

This role involves ensuring strong engineering performance at Contract Manufacturing Organization (CMO) sites, supporting new product introductions, and managing engineering programs for Large Molecule Drug Substance. The position requires expertise in engineering aspects of large molecule drug substance and involves site assessments, capital management, and troubleshooting.

GSK

On-site Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for oncology clinical programs, working closely with cross-functional teams to design robust clinical trials and drive methodological innovation. You will mentor colleagues and contribute to regulatory strategy, using advanced statistical methods and simulations to inform trial design and risk assessment.

GSK

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK

Hybrid Permanent

Global Clinical Study Lead

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

Senior AI Engineer

This role involves designing and delivering end-to-end AI solutions, leading the development of agentic and retrieval-augmented systems, and ensuring robust evaluation and quality. You will work closely with cross-functional teams to turn ambiguous challenges into production-grade AI systems that drive business value and improve patient outcomes.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Clinical Project Manager

As a Clinical Project Manager, you will manage clinical trial packaging and distribution projects from start to finish, acting as the main point of contact for clients and coordinating cross-functional teams. You will ensure projects meet timelines, budgets, and quality standards while maintaining compliance with GMP/GDP requirements and client processes.

Yolk Recruitment Blackwood, Cymru / Wales, United Kingdom £45,000 pa

Hybrid Permanent

Legal Counsel - Pharma/Life Sciences (12-month

Your new companyA global pharmaceutical and life sciences organisation is seeking an experienced Legal Counsel to join its UK & Ireland legal team on a 12-month contract. Operating at the forefront of healthcare innovation, the business develops and delivers medicines,...

Hays Legal Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £450 – £580 pd

Contract

Clinical Data Analytics Lead

As Clinical Data Analytics Lead, you will transform complex clinical trial data into actionable insights, enhancing decision-making and data quality. You will collaborate with cross-functional teams to drive risk-based approaches, improve study oversight, and support patient outcomes using advanced analytics and visualization tools.

Novartis London, United Kingdom

Hybrid Permanent

Director, Development Unit CQA Program Lead

Salary Range:£78,400.00 - £145,600.00Job Description Summary#LI-HybridLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London (The Westworks), United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.Shaping the future of clinical development requires...

Novartis London, United Kingdom

GCP Compliance Manager (GCO)

This role involves leading quality issue management, audit coordination, and inspection readiness for global clinical trials, ensuring compliance with GCP and regulatory standards. The manager will drive self-assessments, conduct risk-based investigations, and provide expert guidance across clinical operations. It’s a high-impact compliance position requiring strong cross-functional influence and operational rigor in a hybrid working environment.

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

Hybrid Permanent

Global Clinical Operations Budget Manager

As a Global Clinical Operations Budget Manager, you will translate complex study assumptions into financial insights, manage budgets and forecasts for clinical trials, and work closely with clinical and finance teams to ensure transparency and accuracy. The role involves partnering across a global matrix environment to drive smarter decisions and optimize trial delivery, ultimately accelerating the development of innovative medicines.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Global Clinical Operations Budget Manager

This role involves managing budgets and financial forecasts for clinical trials, working closely with clinical and finance teams to ensure accuracy and transparency. You will translate complex study assumptions into actionable financial insights, optimize trial delivery, and support process improvements in a global matrix environment.

Novartis London, United Kingdom

Hybrid Permanent

Clinical Quality Assurance - Program Lead (Associate Director)

The Associate Director, Clinical Quality Assurance (QA) will lead quality oversight for clinical trials, ensuring compliance with health authority requirements and patient safety. Responsibilities include implementing quality strategies, monitoring risk management, and supporting governance for quality incidents. The role involves collaboration with key stakeholders and active participation in continuous improvement initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Manager, Content

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels and regulatory guidance, and ensuring compliance with global standards across the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent