Jobs in Leeds

Embedded Software Engineer

This role involves designing and maintaining embedded C/C++ firmware for medical and mechatronic devices, taking full ownership of the software lifecycle, and establishing internal processes such as version control and documentation standards. The engineer will work hands-on with hardware teams, debug using test equipment, and lead the transition of firmware development from external contractors to in-house. It’s a rare opportunity to shape software engineering practices from the ground up within a small, mission-driven team focused on life-changing technology.

YT Technologies Belle Isle, West Yorkshire, WF1 5PS, United Kingdom £45,000 – £60,000 pa

Hybrid Permanent

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL

On-site 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

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

Associate Director, Biostatistics 2

The role involves leading the statistical aspects of clinical development programs, including study design, data analysis, and regulatory submissions. Responsibilities include collaborating with cross-functional teams, managing CROs, and representing Biostatistics in regulatory interactions.

Appcast Enterprise Maidenhead, SL6 1QB, United Kingdom

On-site Permanent

Associate Director, Safety Epidemiology – Global Patient Safety

This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Research Pipeline Project Manager

The Research Pipeline Project Manager will lead and coordinate cross-functional pre-clinical research projects, partnering with scientists and clinical teams to advance scientific priorities. Responsibilities include end-to-end planning, risk management, and driving improvements in team efficiency and transparency.

GSK Stevenage, United Kingdom

Hybrid Permanent

Research Pipeline Project Manager

The Research Pipeline Project Manager will lead and coordinate cross-functional pre-clinical research projects, partnering with scientists and clinical teams to advance scientific priorities. Responsibilities include end-to-end planning, risk management, and driving improvements in project delivery processes, with a focus on patient impact and team collaboration.

GSK

Hybrid Permanent

Precision Medicine Director

The Precision Medicine Director leads biomarker and diagnostic strategy development for global clinical programs in neuroscience, ensuring alignment with regulatory and clinical objectives. This role involves leading cross-functional teams, designing patient selection approaches, and supporting regulatory submissions. The position operates at the intersection of clinical development, diagnostics, and precision medicine, with a strong focus on scientific rigor and compliance.

Novartis London, United Kingdom

Hybrid Permanent

Precision Medicine Director

Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingNovartis is unable to offer relocation support: please only apply if accessible.The Precision Medicine Director is responsible for developing and executing precision medicine strategies aligned to disease area and clinical program objectives. This role leads...

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

Senior Director of Operational Technology (Operations)

This role involves leading the execution of OT strategy across AstraZeneca's global manufacturing network, ensuring alignment with business priorities and improving reliability, safety, and compliance. Key responsibilities include lifecycle management, risk mitigation, capability building, and regulatory readiness.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Head of Health Economics and Outcomes

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 Welwyn Hatfield, United Kingdom

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