Latest IT Consulting Jobs

Research Pipeline Project Manager

The Research Pipeline Project Manager will lead and coordinate cross-functional pre-clinical research projects, partnering with scientists and clinical teams to advance scientific priorities. Responsibilities include end-to-end planning, risk management, and driving improvements in project delivery processes, with a focus on patient impact and team collaboration.

GSK

Hybrid Permanent

Principal Programmer / Analyst

This role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering quality assurance and innovation.

GSK

Hybrid Permanent

Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external drug product manufacturing, coordinating between GSK and Contract Manufacturing Organisations (CMOs) to ensure timely and compliant delivery. The specialist will drive project schedules, mitigate risks, align cross-functional teams, and maintain governance across the supply chain, particularly for sterile drug products like monoclonal antibodies and vaccines. A key focus is ensuring technical knowledge retention and operational readiness for new suppliers or assets.

GSK United Kingdom €69,600 – €116,000 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and data foundations for Supported Studies at GSK, ensuring data integrity, system performance, and compliance. The Associate Director will lead digital integration, dashboard governance, and process improvements, acting as a bridge between business and technology teams to enhance efficiency and regulatory adherence in clinical operations.

GSK United States US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads operational excellence for Supported Studies at GSK, focusing on data integrity, system governance, and digital transformation. The individual will own the data and dashboard ecosystem, act as Business System Owner for key platforms like IdeaPoint and Veeva, and ensure compliance with regulatory requirements such as Transfer of Value. They will bridge business and technology to drive process improvements, enable resource planning, and enhance data transparency across clinical operations.

GSK £154,275 – £257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies program. The Associate Director will lead data governance, system ownership, and digital integration efforts, ensuring data integrity, compliance, and efficiency across platforms like Veeva and IdeaPoint. The position acts as a bridge between business and technology, driving process improvements and digital transformation in a regulated clinical environment.

GSK US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads the operational and digital foundations for Supported Studies at GSK, ensuring data integrity, system performance, and compliance across platforms like Veeva and IdeaPoint. The individual will drive process improvements, support regulatory reporting such as Transfer of Value, and act as a bridge between business and technology teams to enhance efficiency and scalability in clinical operations.

GSK US$154,275 – US$257,125 pa

Hybrid Permanent

Project Specialist (External Manufacturing-Drug Product)

The role involves managing technology transfer projects for external manufacturing of drug products, coordinating between GSK and Contract Manufacturing Organisations (CMOs). The specialist ensures timely delivery of critical path activities, aligns internal and external stakeholders, and maintains governance across procurement, quality, technical, and supply functions, particularly for sterile drug products like monoclonal antibodies and vaccines.

GSK €69,600 – €116,000 pa

Hybrid Permanent

Director, Global RWE-HO, Oncology

Leads the planning, design, and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across the product lifecycle. Collaborates with cross-functional teams to generate robust evidence for regulatory, reimbursement, and market access decisions. Focuses on translating clinical and economic value into impactful data for payers, providers, and patients.

GSK United States

Hybrid Permanent

Director, Global RWE-HO, Oncology

This role involves leading the design and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across their lifecycle. The Director will develop robust data generation plans, align evidence with regulatory and payer requirements, and collaborate with cross-functional teams and external experts to ensure impactful evidence for market access and patient outcomes. The position plays a strategic role in shaping value propositions through scientifically credible research in a global, matrix environment.

GSK

Hybrid Permanent

Director, Global RWE-HO, Oncology

Leads the design and execution of real-world evidence and health outcomes studies to support oncology assets, ensuring robust data generation for regulatory, reimbursement, and market access decisions. Collaborates across medical, commercial, and R&D teams to align evidence strategies with global customer needs and health technology assessment requirements. Engages with external experts and internal stakeholders to deliver high-impact scientific research throughout the product lifecycle.

GSK

Hybrid Permanent

Director, Government Affairs and Advocacy - Europe and International

Director, Government Affairs and Advocacy – Europe and International ViiVAbout ViiVWe are a specialist pharmaceutical company 100% dedicated to developing medicines to treat and prevent HIV. As the pioneers in HIV innovation, we constantly look to push the boundaries of...

GSK United Kingdom

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, manufacturability, and regulatory compliance by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives across the global supply chain.

GSK United States

Hybrid Permanent

Product Owner, Clinical Trial Site Management

This role involves leading AI-first product development for clinical trial site management systems at GSK, focusing on transforming how trials are conducted from feasibility through close-out. The Product Owner will drive strategy, adoption, and innovation across site-facing and internal operational platforms, using AI to enhance processes like contracting, budgeting, and monitoring. The role emphasizes responsible AI integration in a regulated GxP environment, with strong stakeholder collaboration across R&D operations and technology teams.

GSK United Kingdom

Hybrid Permanent

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. The Director will guide cross-functional teams in designing and validating digital biomarkers, collaborating with external partners, and enhancing the efficiency and patient-centricity of GSK's clinical trials.

GSK

On-site Permanent