Latest Medical Affairs Partner - Nephrology & R Jobs

Disease Level Partner - South Central UK

The Disease Level Partner (DLP) is responsible for implementing Roche's strategy and objectives within therapy areas, focusing on patient outcomes. Key responsibilities include deep customer engagement, gathering actionable insights, and driving positive customer experiences. The role involves leveraging resources to secure access for key customers and contributing to the development of local and national brand advocates.

Roche United Kingdom

On-site Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing processes to generate high-quality medical insights. Key responsibilities include developing strategies, prioritizing use cases, and applying advanced analytics and AI to inform medical decision-making. The role also focuses on embedding insights into core medical processes and collaborating with various stakeholders to ensure effective use of insights.

Pfizer

On-site 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 leveraging advanced analytics and AI to translate complex medical data into strategic decisions, ensuring consistency and value across Pfizer’s medical portfolio.

Pfizer

On-site Permanent

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leading the implementation of Medical Affairs processes, and supporting transversal business prioritization. You will work closely with Local Operating Companies to ensure effective communication, conduct impact assessments, and support data generation processes, including Investigator-Sponsored Studies and Real World Evidence initiatives.

GSK

On-site Permanent

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leading the implementation of Medical Affairs processes, and supporting data generation across the EU and International regions. You will collaborate with local operating companies, conduct impact assessments, and serve as a subject matter expert in innovative processes.

GSK

On-site Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, leading resource planning, and representing the function in senior interactions and health authority meetings.

AstraZeneca United States

On-site 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 shaping labelling content, ensuring regulatory compliance, and collaborating with cross-functional teams to support successful product submissions and patient safety.

Novartis London, United Kingdom

Hybrid 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 Study Lead

The Global Study Lead is responsible for managing the full lifecycle of clinical studies, from design and planning to execution and documentation. Key responsibilities include leading the study team, ensuring compliance with regulations, managing budgets, and collaborating with cross-functional teams and external partners to deliver high-quality study results.

Roche United States

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 Affairs Specialist - Medical Devices

This role involves leading quality assurance and regulatory affairs initiatives within a global medical devices company, working across European, American, and Asian regulatory standards. You will develop and implement solutions for compliance and management systems in a highly technical R&D and manufacturing environment. The position offers exposure to emerging regulated industries and complex, international projects.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £42,000 – £46,000 pa

On-site Permanent

Regulatory Affairs Manager

Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business...

Cure Talent Curbridge, Oxfordshire, Oxfordshire, United Kingdom £85,000 – £95,000 pa

Regulatory Affairs Specialist

This role involves maintaining technical documentation and ensuring compliance with UK and EU MDR regulations for Class I and IIa medical devices. The specialist will support regulatory submissions, post-market surveillance, and quality management system development within a regulated environment. Collaboration with the QA Manager and ongoing product lifecycle support are key aspects of the position.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Regulatory Affairs Manager EU & US

This role involves leading regulatory strategy for EU and US markets within a pharmaceutical CDMO, managing submissions to EMA and FDA, and overseeing regulatory documentation for complex drug products. The candidate will act as a key liaison with global regulatory agencies and lead a small team, contributing to lifecycle management and regulatory intelligence. The position requires deep expertise in centralised procedures, dossier compilation, and cross-functional collaboration in a fast-paced environment.

Hays Life Sciences Cheshire, United Kingdom

Hybrid Permanent