Latest Pharmaceutical Scientist Jobs

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

Trial Master File Oversight Manager

This role involves overseeing the quality and completeness of Trial Master Files across global clinical trials, ensuring compliance and readiness for audits. The manager will lead vendor oversight, identify documentation risks, and drive process improvements while acting as a subject matter expert. Collaboration with cross-functional teams is essential to maintain high standards in clinical documentation and support continuous innovation in TMF systems.

Novartis London, United Kingdom £49,140 – £91,260 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

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on ensuring compliance and timely approval of new and marketed products, serving as a regulatory liaison throughout the product lifecycle.

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

Director, Clinical Trial and Data Transparency

This role involves providing strategic and operational expertise for the disclosure of clinical regulatory documents on public websites, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes and technologic solutions to support transparency in clinical trials.

Pfizer India

Remote Permanent

Director, Clinical Trial and Data Transparency

This role involves leading the strategic and operational aspects of clinical trial transparency and disclosure, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes for compliance.

Pfizer

Remote Permanent

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Responsibilities include driving technology strategy, implementing AI and automation, shaping GTCS-related changes, enabling data-driven decision-making, and ensuring compliance and risk management.

Pfizer Spain

On-site Permanent Flexible

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Key responsibilities include driving technology strategy, leading AI and automation initiatives, shaping GTCS-related technology changes, and enabling data-driven decision-making to support strategic and operational insights.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Global Labelling Manager, Content (Neuroscience)

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 ensuring compliance with regulatory standards across different markets.

Novartis

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

Senior Principal Developer

This role involves developing and maintaining R packages and Shiny applications to support clinical trial data analysis, automation, and reporting workflows. The developer will collaborate with statisticians and clinical teams to deliver efficient, reproducible tools, while promoting best practices in data science and software development. A strong focus is placed on responsible AI integration, open-source collaboration, and modernizing clinical reporting through user-centric design and tooling.

Novartis London, United Kingdom £57,050 – £105,950 pa

Hybrid Permanent