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Senior Medical Manager - Medial Affairs UK & I

The Senior Medical Affairs Manager is a key scientific leader responsible for external engagement with key opinion leaders, healthcare organizations, and policy stakeholders. The role involves developing and executing the UK Medical Affairs strategy, leading scientific exchanges, and representing Seqirus at national scientific forums. The position also focuses on internal collaboration, evidence generation, and ensuring compliance with regulatory standards.

CSL United Kingdom £70,000 – £100,000 pa

On-site Permanent

Associate Director, R&D Project Management

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

Hybrid 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 £40,000 – £60,000 pa

On-site Permanent

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development of a medicine for cardiovascular and renal conditions, including strategic planning, team leadership, and ensuring compliance with regulations. The position requires significant clinical and scientific oversight, authoring key documents, and collaborating with cross-functional teams to drive the program's success.

CSL

On-site Permanent

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development of a medicine for cardiovascular and renal conditions, including strategic planning, team leadership, and ensuring compliance with regulations. The position requires significant clinical and scientific oversight, authoring key documents, and collaborating with cross-functional teams to drive the program's success.

CSL Switzerland

On-site Permanent