Jobs in Stoke-on-trent

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

The Medical Director role at ViiV Healthcare focuses on managing and overseeing Phase 1-4 clinical trials, ensuring the successful planning, execution, and reporting of protocols. Key responsibilities include providing medical governance, managing safety events, and collaborating with internal and external stakeholders to develop groundbreaking HIV treatments.

GSK

On-site Permanent

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leveraging medical platforms, and leading the implementation of 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 such as investigator-sponsored studies and real-world evidence.

GSK United Kingdom

On-site Permanent

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Oxford, United Kingdom

On-site Permanent

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna

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. The role requires strong project management skills, knowledge of HIV, and the ability to work independently and collaboratively with diverse teams.

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. 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

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

Clinical Sciences Manager, Global Collaborative Studies – ViiV Healthcare 10 month maternity cover

This role involves leading and managing ViiV Healthcare's supported studies, including investigator-sponsored and collaborative studies. Responsibilities include reviewing study proposals, ensuring compliance with policies, and maintaining strong relationships with external investigators and internal stakeholders.

GSK United Kingdom

On-site Temporary

Clinical Sciences Manager, Global Collaborative Studies – ViiV Healthcare 10 month maternity cover

This role involves leading and managing ViiV Healthcare's supported studies, including investigator-sponsored and collaborative studies. Responsibilities include managing study proposals, ensuring compliance, and building relationships with external investigators and internal stakeholders. The role is crucial for generating evidence to inform HIV treatment and advancing ViiV's mission.

GSK

On-site Temporary

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to protocol development, and providing medical oversight and support. You will work closely with internal and external stakeholders to ensure the successful execution and interpretation of clinical studies, with a focus on advancing HIV treatments and prevention.

GSK United Kingdom

On-site Permanent

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to the design and medical governance of studies, and providing medical expertise and support throughout the trial process. The role is crucial in advancing HIV treatments and working closely with internal and external stakeholders to ensure the success of clinical studies.

GSK

On-site Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

Moderna London, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading regulatory discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

Moderna

On-site Permanent