Latest IT Consulting Jobs

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Scientist, Analytical Operations - Small Molecule Stability Data Management

This role involves managing and improving stability data for small molecule studies, creating and maintaining study protocols, and producing clear data visualizations for regulatory submissions. You will work closely with cross-functional teams and external partners to drive process improvements and ensure data integrity.

GSK Stevenage, United Kingdom
Hybrid Permanent
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Scientist, Analytical Operations - Small Molecule Stability Data Management

In this role, you will manage and improve stability data for small molecule studies, create and maintain study protocols, collect and analyse datasets, and produce clear summaries and visualisations for regulatory submissions. You will also support audits, collaborate with cross-functional teams, and drive process improvements through digital tool adoption.

GSK East Hertfordshire, United Kingdom
Hybrid Permanent
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Senior Specialist, Data Science

Job Title: Senior Specialist, Data Science — Operational Data Strategy (ODS), BioPharma R&DLocation: United KingdomCompetitive Salary & Excellent Company Benefits!Introduction to the Role:The Operational Data Strategy (ODS) function provides strategic oversight for how clinical operations data is collected, organized, validated,...

AstraZeneca Cambridge, United Kingdom
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Associate Director, Operations Excellence Supported Studies

This role leads operational excellence for Supported Studies at GSK, focusing on data governance, system ownership, and digital integration. The individual will ensure data integrity, drive compliance with regulatory requirements like Transfer of Value, and translate operational needs into scalable digital solutions. Working across cross-functional teams, they will enhance efficiency, quality, and transparency in clinical operations through robust dashboards, automation, and process improvements.

GSK Stevenage, United Kingdom US$154,275 – US$257,125 pa
Hybrid Permanent
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Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies, ensuring data integrity, system performance, and compliance. The individual will lead data governance, dashboard development, and system integration—particularly for platforms like Veeva and IdeaPoint—while acting as a bridge between business and technology teams to drive efficiency and compliance in clinical study delivery.

GSK London, United Kingdom US$154,275 – US$257,125 pa
Hybrid Permanent
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Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external contract manufacturing organizations (CMOs) in the pharmaceutical sector, ensuring alignment between GSK and suppliers on timelines, quality, and technical deliverables. The specialist will coordinate cross-functionally across procurement, quality, technical, and supply teams to operationalize new assets or suppliers, with a focus on sterile drug products like monoclonal antibodies and vaccines. Key responsibilities include maintaining critical path schedules, mitigating risks, and driving project governance from transfer through to product launch.

GSK Worthing, United Kingdom €69,600 – €116,000 pa
Hybrid Permanent
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Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external contract manufacturing organizations in the pharmaceutical sector, ensuring alignment between GSK and suppliers. The specialist will oversee project schedules, mitigate risks, and ensure timely delivery of drug products across critical assets like monoclonal antibodies, vaccines, and small molecules. Collaboration with cross-functional teams and supplier relationship management are central to driving successful operationalization within budget and timeline.

GSK East Hertfordshire, United Kingdom €69,600 – €116,000 pa
Hybrid Permanent
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Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external drug product manufacturing with Contract Manufacturing Organisations (CMOs). The specialist will coordinate cross-functionally across Procurement, Quality, Technical, and Supply teams to establish and maintain project schedules, mitigate risks, and ensure timely delivery of assets within budget. The position emphasizes strong stakeholder engagement, governance, and retention of manufacturing knowledge across the supply network.

GSK Durham, DH1 3NG, United Kingdom €69,600 – €116,000 pa
Hybrid Permanent
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Scientist in Translational Pathology, Oncology

This role involves working in a lab-based GCP environment, supporting translational pathology and biomarker programs. Responsibilities include maintaining quality standards, managing clinical and research specimens, performing laboratory assays, and collaborating with cross-functional teams to ensure laboratory activities align with project needs.

AstraZeneca Cambridge, United Kingdom
On-site Permanent
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Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through commercial manufacturing. The Molecule Steward ensures product quality, robustness, and manufacturability by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives. It requires deep scientific expertise, regulatory knowledge, and strong collaboration across R&D, manufacturing, and supply chain functions.

GSK Worthing, United Kingdom
Hybrid Permanent
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Molecule Steward

This role involves providing strategic technical leadership for a pharmaceutical product across its entire lifecycle, from development through manufacturing and commercial supply. The Molecule Steward ensures product quality, robustness, and compliance by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives. It requires deep scientific expertise, regulatory knowledge, and strong collaboration across R&D, manufacturing, and supply chain functions.

GSK Barnard Castle, United Kingdom
Hybrid Permanent
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Molecule Steward

This role involves leading the technical strategy for a pharmaceutical product across its lifecycle, from development through manufacturing and commercial supply. The Molecule Steward ensures product quality, regulatory compliance, and process robustness by coordinating cross-functional teams and maintaining the Product Control Strategy. It requires deep scientific expertise, leadership in technical decision-making, and strong collaboration across R&D, manufacturing, and regulatory functions.

GSK East Hertfordshire, United Kingdom
Hybrid Permanent
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Product Performance Lead (Team-Manager)

Lead a technical team at GSK’s Ware manufacturing site to monitor and improve product performance across respiratory and oral solid dose medicines. Drive the local execution of the technical lifecycle plan, lead investigations into manufacturing issues, and implement process improvements using lean methodologies and digital tools. Collaborate with global MSAT stewards and site leadership to ensure compliance, efficiency, and innovation in a highly regulated environment.

GSK East Hertfordshire, United Kingdom
On-site Permanent
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Director, Digital Medicine: Respiratory, Immunology & Inflammation Research Unit

This role involves shaping digital medicine strategies and leading the development of digital tools to support the safe use of medicines in respiratory, immunology, and inflammation research. You will collaborate with cross-functional teams to design and validate digital biomarkers, enhance clinical trials, and engage external partnerships to accelerate capability and delivery.

GSK Stevenage, United Kingdom
On-site Permanent
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Director, Digital Medicine: Respiratory, Immunology & Inflammation Research Unit

This role involves leading the development and implementation of digital medicine strategies to support clinical programs and studies in respiratory, immunology, and inflammation. You will work across various teams to design and validate digital biomarkers, enhance clinical trials with AI, and collaborate with external partners to accelerate capability and delivery.

GSK London, United Kingdom
On-site Permanent