Latest Business Insights Manager Jobs

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, managing submissions and approvals, and driving continuous improvement and innovation.

GSK

Hybrid Permanent

Director Medical Writing Process Management

The Director Medical Writing Process Management will lead the optimization of end-to-end business processes within Medical Writing, ensuring compliance, efficiency, and continuous improvement. They will collaborate with cross-functional teams to implement best practices, monitor process health, and align with GSK’s strategic goals.

GSK Stevenage, United Kingdom

On-site Permanent

End-to-End Product Lead, AMP

This role involves leading the development and delivery of an intelligent content operating system called AMP, which connects how marketers plan, create, review, and measure content. The Product Lead will define the product vision, roadmap, and success metrics, manage a team of product owners, and collaborate with stakeholders across content strategy, operations, design, engineering, data, and compliance to ensure alignment and drive measurable outcomes in user productivity, quality, and compliance.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

End-to-End Product Lead, AMP

The AMP Product Lead is responsible for defining and executing the vision, strategy, and roadmap for an intelligent content operating system. This role involves close collaboration with global stakeholders to ensure alignment across marketing and technology, driving measurable outcomes in productivity, quality, and compliance.

Pfizer

Remote Permanent

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership on complex strategic topics, optimize investment decisions, and collaborate across functions to deliver impactful patient outcomes.

AstraZeneca

On-site Permanent

Director, AI Research

This role involves leading AI research to accelerate drug development and improve patient outcomes by guiding a high-calibre team in inventing and applying advanced machine learning methods. The Director will set the research agenda, convert scientific advances into production-grade models, and ensure robust ML governance while collaborating with cross-functional teams.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Regulatory Manager

As a Regulatory Manager, you will lead regulatory strategy for drug-device combination products, working closely with global regulatory bodies and clients. You will manage a small team, review key documentation, and contribute to regulatory intelligence, with opportunities for career growth in a forward-thinking, innovative company.

Hays Life Sciences Cheshire, United Kingdom

On-site Permanent

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

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

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 activities, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna

On-site Permanent

Field Service Engineer (Omagh, Enniskillen, border regions)

This role involves providing frontline technical support for Roche's diagnostic products in the Omagh, Enniskillen, and border regions. Responsibilities include troubleshooting, preventative maintenance, technical training, and ensuring regulatory compliance. The position emphasizes customer satisfaction and continuous improvement.

Roche United Kingdom

On-site Permanent

Field Service Engineer (Omagh, Enniskillen, border regions)

This role involves providing frontline technical support for Roche's diagnostic products in the Omagh, Enniskillen, and border regions. Responsibilities include troubleshooting, preventative maintenance, technical training, and ensuring regulatory compliance. The position requires a strong technical background and the ability to work effectively in a fast-paced, customer-focused environment.

Roche

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

Regulatory Affairs Specialist - Medical Devices - Cambridge

This role involves providing regulatory expertise to guide product development across medical and non-medical technologies, ensuring compliance with international standards such as ISO 13485, FDA 21 CFR 820, and ISO 9001. The specialist will work embedded within project teams, interpreting evolving regulations, supporting quality systems, and enabling innovation while maintaining regulatory alignment throughout the product lifecycle.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent