Latest regulatory affairs 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 cross-functional alignment to deliver best-in-class regulatory outcomes.

GSK

Hybrid Permanent

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

Head of Medical & Scientific Affairs - Cardiovascular, Renal & Metabolic

Leads national medical strategy for cardiovascular, renal, and metabolic therapies, shaping policy, driving NHS collaborations, and accelerating patient access to innovative treatments. Champions real-world evidence, scientific launch readiness, and cross-functional medical execution across the UK healthcare system.

AstraZeneca London, United Kingdom

Hybrid 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

Global Labelling Director, Content

The Global Labelling Director, Content will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include shaping labelling content, maintaining core documents, and collaborating with cross-functional teams to ensure regulatory compliance and successful product submissions.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Director, Content (Immunology)

The Global Labelling Director, Content (Immunology) will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include developing core labelling documents, collaborating with cross-functional teams, and ensuring compliance with regulatory requirements. The role involves representing global labelling in governance forums and contributing to decision-making discussions.

Novartis

Hybrid Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing Medical Insights processes, collaborating with various stakeholders to generate actionable insights, and embedding these insights into medical decision-making. The role focuses on advanced analytics, AI, and emerging technologies to drive value and impact across Pfizer’s medical portfolio.

Pfizer United States

On-site Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing processes to generate and apply high-quality medical insights across Pfizer. Key responsibilities include developing Medical Insights strategies, prioritizing use cases, translating complex data into actionable insights, and embedding these insights into core medical processes to support informed decision-making and strategic discussions.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Associate Director, Resilience Strategic Partnerships – UK

This role involves leading the execution of Moderna's strategic partnership with the UK government, focusing on mRNA-based vaccines and biomanufacturing. You will manage day-to-day interactions with key government stakeholders, represent Moderna on the UKHSA operations board, and drive cross-functional collaboration to deliver on program objectives and commitments.

Moderna London, United Kingdom

On-site Permanent

Associate Director, Resilience Strategic Partnerships – UK

This role involves leading the execution of Moderna's strategic partnership with the UK government, focusing on mRNA-based vaccines and biomanufacturing. You will manage day-to-day interactions with key government stakeholders, represent Moderna on the UKHSA operations board, and drive cross-functional collaboration to deliver public health impact.

Moderna Tameside, SK15 3JG, United Kingdom

On-site Permanent

Principal Scientist – Histopathology

This role involves leading technical aspects of assay and product development in histopathology, with a focus on immunohistochemistry (IHC) slide interpretation and scoring. The Principal Scientist will provide strategic direction, mentor junior scientists, and collaborate across R&D, quality, and regulatory teams to advance diagnostic tools. Expertise in regulated environments and digital pathology is highly valued.

Taylorollinson Newcastle upon Tyne, Tyne & Wear, NE1 4JA, United Kingdom £50,000 – £60,000 pa

On-site Permanent

Regulatory Science Professional - Intelligence

This role involves managing regulatory intelligence for Roche’s pharmaceutical and medical device portfolio in the EU, with a focus on generating strategic, data-driven insights. The professional will leverage AI tools, maintain regulatory databases, and collaborate across global teams to inform decision-making and drive innovation in a dynamic regulatory environment.

Roche Welwyn Hatfield, 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

Medical Device Programme Lead

Balance technical, regulatory and commercial challenges in this fulfilling roleThis highly regraded Cambridge-based medical technologies company is seeking a proven engineering leader to help guide high-value development programmes from concept through to transfer to manufacture. Your leadership will accelerate development...

ECM Selection Cambridge, Cambridgeshire, United Kingdom £75,000 – £95,000 pa

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, ensuring appropriate methodologies for study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing operations, and represent Biostatistics in regulatory interactions.

CSL United Kingdom

On-site Permanent