Jobs in Reading

ViiV Healthcare (GSK) Clinical Development Director

The Clinical Development Director at ViiV Healthcare will lead the scientific strategy and execution of clinical development programs for HIV treatments. This role involves designing and overseeing high-quality clinical studies, collaborating with cross-functional teams, and ensuring regulatory compliance and safety monitoring. The position offers a unique opportunity to contribute to groundbreaking HIV research and make a significant impact on patient lives.

GSK United States

On-site Permanent

Senior Regulatory Managers

This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams, provide regulatory advice, and manage interactions with regulatory authorities, ensuring compliance and supply continuity.

GSK

Hybrid Permanent

Principal Statistical Programmer

The Principal Statistical Programmer leads statistical programming activities for large or pivotal clinical studies, ensuring high-quality and timely deliverables. They collaborate with cross-functional teams, mentor other programmers, and maintain compliance with industry standards.

Novartis London, United Kingdom

On-site Permanent

Senior Principal Statistical Programmer

The Senior Principal Statistical Programmer leads statistical programming activities for multiple clinical studies or large projects, ensuring high-quality and timely deliverables. They collaborate with biostatistics, coordinate programming teams, and maintain compliance with industry standards.

Novartis London, United Kingdom

On-site Permanent

ViiV Healthcare (GSK) Clinical Development Manager

The Clinical Development Manager at ViiV Healthcare provides scientific leadership and direction for clinical development programs, focusing on the design and execution of high-quality studies. This role involves collaborating with cross-functional teams to ensure study protocols meet strategic objectives, overseeing data collection and analysis, and contributing to regulatory reporting and scientific outputs.

GSK United States

On-site Permanent

ViiV Healthcare (GSK) Clinical Development Manager

The Clinical Development Manager at ViiV Healthcare is responsible for providing scientific leadership and direction in the design and development of high-quality clinical studies. This role involves collaborating with cross-functional teams to ensure the accuracy and timeliness of study results, contributing to regulatory reporting, and creating scientific outputs for publications and presentations.

GSK

On-site Permanent

Pharmacovigilance Quality Assurance Director

This senior role involves leading and maintaining a robust pharmacovigilance quality assurance programme, ensuring compliance with global regulations and internal standards. Key responsibilities include overseeing PV processes, managing audits, and providing strategic guidance to ensure patient safety and continuous improvement.

GSK United Kingdom

Hybrid Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Leads clinical operations strategy and delivery across Hepatology, Renal, and Cardiovascular disease portfolios, managing a matrix team to ensure high-quality, on-time execution from early phase through lifecycle management. Drives data-informed decision-making, risk mitigation, and innovation adoption while aligning with enterprise goals and regulatory standards.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Lead clinical operations strategy for Hepatology, Renal, and Cardiovascular disease portfolios within GSK's R&D engine. Drive end-to-end delivery of global clinical assets, manage high-performing teams, and ensure operational excellence across phases I–IV. Champion data-driven decision-making, inspection readiness, and innovation while aligning with enterprise goals and shaping future development operations.

GSK United Kingdom US$242,550 – US$404,250 pa

Hybrid Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

This role leads clinical operations strategy and delivery for GSK's Hepatology, Renal, and Cardiovascular disease portfolio, overseeing end-to-end development from early phase through post-marketing. The leader will manage a matrix team, drive operational excellence, embed data-driven decision-making, and align with enterprise goals to ensure high-quality, efficient clinical delivery across global programs.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Product Manager - Regulatory Vault

Are you passionate about making impactful contributions to the world of medicines and vaccines? GlaxoSmithKline (GSK) invites you to join our dynamic R&D Digital and Tech Team as a Product Manager - Regulatory Vault. In this pivotal role, you will...

GSK United Kingdom

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Leads clinical operations strategy and delivery for GSK's Hepatology, Renal, and Cardiovascular disease portfolio, overseeing end-to-end development from early phase through phase IV. Responsible for shaping operational direction, managing cross-functional teams, driving data-led decision-making, and ensuring alignment with enterprise goals. Focuses on innovation, risk management, and talent development within a global R&D environment.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Commercial Operations Director, ViiV UK

Leads UK commercial operations for ViiV Healthcare, driving marketing strategy, cross-functional projects, and operational performance across the HIV portfolio. Focuses on customer engagement, launch readiness, and data-driven decision-making in close collaboration with sales, medical, and market access teams.

GSK United Kingdom

Hybrid Permanent

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and clear communication. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory compliance and process improvement.

GSK United States

On-site Permanent

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and compliance. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory submissions and process improvements.

GSK

On-site Permanent