Latest Medical Affairs Partner - Nephrology & R Jobs

Medical Affairs Partner - Nephrology & Rheumatology

This role involves leveraging medical and scientific expertise to shape and drive strategic initiatives within Medical Affairs for Nephrology and Rheumatology in the UK. The individual will translate complex data into actionable insights, engage with healthcare experts, and support both local and global projects aimed at improving patient outcomes. Collaboration across teams and contribution to high-impact medical strategies are central to the position.

Roche

Hybrid Contract

Medical Affairs Partner - Nephrology & Rheumatology

This role involves shaping and driving medical affairs strategy in Nephrology and Rheumatology by translating complex scientific data into actionable insights. The Medical Affairs Partner will collaborate with internal teams and external healthcare experts to support patient outcomes, leveraging deep medical expertise and building scientific partnerships. The position emphasizes strategic initiative leadership and stakeholder engagement within the UK affiliate and global context.

Roche

Hybrid 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

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, leveraging medical platforms, and aligning medical affairs processes across the EU and International regions. Responsibilities include supporting transversal business prioritization, improving communication with local operating companies, and assisting with data generation processes and investigator-sponsored studies.

GSK

On-site Permanent

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leveraging medical platforms, and aligning medical affairs processes across the EU and International regions. Key responsibilities include supporting transversal business prioritization, improving communication with local operating companies, and assisting with data generation processes and real-world evidence studies.

GSK

On-site Permanent

PV Systems and Processes Lead x2

This role involves maintaining and improving CSL's global pharmacovigilance (PV) system, ensuring compliance with GVP and regulatory requirements. Responsibilities include leading investigations, managing deviations, coordinating inspections, and providing PV training across various functions and affiliates.

CSL United Kingdom

On-site Permanent

Quality and Regulatory Labelling Program Manager

This role involves leading global labelling initiatives to ensure compliance with regulatory standards across multiple markets. The Program Manager will work closely with cross-functional teams to manage change controls, mitigate risks, and drive continuous improvement in labelling processes.

Randstad Engineering Popley, Hampshire, RG24 9TW, United Kingdom £27 ph

Hybrid Contract

Medical Affairs Lead - Lung

This role involves leading the medical input for AstraZeneca's Lung Oncology portfolio, developing and delivering medical plans, and maintaining scientific relationships with key customers. The Medical Affairs Lead will also ensure regulatory compliance and support market access activities, working closely with the Therapy Area Medical Team to drive innovation and excellence.

AstraZeneca London, United Kingdom

Hybrid Permanent

Executive Medical Director

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom

Hybrid Permanent

Senior Scientific Engagement & Program Manager

This role involves planning and executing high-quality medical and scientific engagement activities across various therapeutic areas, including Oncology, Cardiovascular Disease, and Immunology. The Senior Scientific Engagement & Program Manager will coordinate advisory boards, congress activities, and medical education programs, ensuring seamless delivery and continuous improvement in processes and tools.

Novartis London, United Kingdom

Hybrid Permanent

Senior Scientific Writer II

The Senior Scientific Writer II role involves developing high-quality medical and scientific communications for Novartis, including slide decks, congress materials, and advisory board content. The position requires strong collaboration with cross-functional teams to ensure content accuracy, consistency, and compliance with internal and external standards.

Novartis London, United Kingdom

Hybrid Permanent

Associate / Senior General Counsel

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom

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, and representing the function in senior interactions and health authority meetings.

AstraZeneca Canterbury, United Kingdom

On-site Permanent

Associate Director, Regulatory Affairs

This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent