Jobs in Reading

Site Shift Manager

This role involves leading 24/7 manufacturing operations outside core hours at GSK’s Barnard Castle site, ensuring safety, compliance, and supply chain continuity. The Site Shift Manager acts as the primary on-site leader during shifts, coordinating production, managing incidents, and aligning cross-functional teams including manufacturing, quality, and engineering. Emphasis is placed on real-time decision-making, audit readiness, and continuous improvement in a regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Operations NPI Technologist

This role involves leading the integration of new equipment, processes, and technologies into sterile manufacturing operations, ensuring compliance, safety, and minimal disruption to supply. The technologist will work across project lifecycles—from design and validation to handover—providing technical leadership and operational readiness support. Collaboration with engineering, quality, and digital manufacturing teams is key to deploying capital projects and new product introductions in a GMP-regulated environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays (including RT-qPCR, dPCR, and NGS) to support clinical biomarker programs across Moderna’s therapeutic pipeline. The scientist will drive end-to-end assay lifecycle management, ensure regulatory compliance with GCLP standards, and collaborate with cross-functional teams to generate high-quality genomic data for clinical decision-making. Emphasis is placed on innovation, data integrity, and integrating emerging technologies like AI-enabled tools to accelerate translational research.

Moderna

Hybrid Permanent

Senior Automation Engineer, Laboratory Automation & Biobanking

This role involves designing and optimizing automated laboratory workflows for biomarker testing and sample management within Moderna’s Clinical Biomarker Laboratory. The engineer will lead integration of advanced liquid handling systems, develop data pipelines, and ensure compliance with regulatory standards, while collaborating across digital, operations, and vendor teams to build scalable, AI-enhanced automation platforms.

Moderna

Hybrid Permanent

Global Labelling Associate Director, Content (Established Products)

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

Director, Medical Insights

The Director, Medical Insights role at Pfizer involves shaping and implementing Medical Insights processes, collaborating with various stakeholders, and leveraging advanced analytics and AI to translate complex medical data into actionable insights. The role focuses on embedding these insights into medical decision-making and strategic discussions, ensuring they are relevant and impactful across Pfizer’s portfolio of medicines.

Pfizer

Remote Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing strategies to enhance Pfizer's medical insights capabilities. Key responsibilities include developing insights frameworks, driving alignment across medical affairs, and leveraging advanced analytics and AI to translate complex data into actionable insights that inform strategic decisions.

Pfizer

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position shapes operational strategy, drives innovation in trial design, and ensures delivery across a diverse asset portfolio. It involves leading vendor partnerships, managing regulatory and quality compliance, and developing clinical teams within a patient-ambitious, data-driven environment.

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

Hybrid Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for complex, multi-indication assets in hepatology, renal, and cardiovascular disease, with strategic oversight of global Phase III trials, rare disease programmes, and co-development partnerships. The position involves shaping operational strategy, managing high-level vendor relationships, and driving innovation in trial design including decentralised and hybrid models. It requires leadership in risk management, data-driven decision-making, and team development within a global regulatory and compliance framework.

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

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-complexity assets in hepatology, renal, and cardiovascular disease, with a focus on global Phase III outcomes trials, rare disease programmes, and co-development partnerships. The position drives end-to-end operational strategy, including country and site selection, patient recruitment, risk management, and vendor oversight, while ensuring alignment with clinical development and evidence generation plans. It also involves direct leadership of clinical teams, fostering innovation in trial design, and maintaining inspection readiness across the portfolio.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position involves shaping operational strategy, managing CRO partnerships, and driving innovation in trial design while ensuring quality and compliance. Leadership includes direct management of clinical teams and strategic input into asset development across the R&D pipeline.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for complex, high-impact assets in hepatology, renal, and cardiovascular disease, with responsibility for global Phase III trials, rare disease programmes, and co-development partnerships. The position involves setting operational strategy, managing CROs and vendors, driving data-led decision-making, and ensuring trial delivery to time, cost, and quality. It also includes direct leadership of clinical operations teams and integration of innovative trial methodologies.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-complexity assets in hepatology, renal, and cardiovascular disease, with a focus on global Phase III outcomes trials, rare disease programmes, and co-development partnerships. The position drives operational strategy, risk management, and innovation in trial design, while managing senior vendor relationships and developing clinical teams. It emphasizes data-led decision-making, enterprise-wide impact, and compliance across a global development portfolio.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Vendor Start-Up Manager - eCOA & Translations

The Vendor Start-Up Manager for eCOA and Translations ensures vendors are aligned and ready to deliver, protecting study timelines, quality, and patient experience. Key responsibilities include technical expertise, risk assessment, continuous improvement, and vendor oversight.

Novartis

Hybrid Permanent