Latest IT Consulting Jobs

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

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 digital biomarkers, endpoints, and measures, and collaborate with external partners to enhance clinical trial efficiency and patient-centric outcomes.

GSK Exeter, EX4 4HD, United Kingdom

On-site Permanent

Principal Medical Writer

The Principal Medical Writer will author and deliver high-quality clinical regulatory documents, lead cross-functional teams in developing clinical dossier documents for global regulatory submissions, and manage complex writing projects. They will interpret complex clinical and statistical information, ensuring compliance with GSK standards and regulatory requirements.

GSK

Hybrid Permanent

Interventional Study Scientist Medical Director

Interventional Study Scientist Medical DirectorLocations– GSK HQ UK, New Oxford Street & USA - Upper Providence/ Waltham MAReports to: Head of Interventional & Supported StudiesJoin GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific...

GSK United Kingdom

Interventional Study Scientist Medical Director

Interventional Study Scientist Medical DirectorLocations– GSK HQ UK, New Oxford Street & USA - Upper Providence/ Waltham MAReports to: Head of Interventional & Supported StudiesJoin GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific...

GSK

Interventional Study Scientist Medical Director

Interventional Study Scientist Medical DirectorLocations– GSK HQ UK, New Oxford Street & USA - Upper Providence/ Waltham MAReports to: Head of Interventional & Supported StudiesJoin GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific...

GSK

SERM Medical/Scientific Director

This role involves providing medical and scientific leadership in the safety evaluation and risk management of ViiV assets during clinical development. The individual will interpret safety data, identify and escalate safety signals, and deliver evidence-based recommendations to inform benefit-risk decisions. They will lead cross-functional teams, contribute to global regulatory submissions, and represent GSK in interactions with regulatory authorities, ensuring patient safety and shaping the safety profile of innovative specialty medicines.

GSK United Kingdom

Hybrid Permanent

Associate Director, Resilience Strategic Partnerships – UK

This role involves leading the execution of Moderna's strategic partnership with the UK government, focusing on mRNA-based vaccines and biomanufacturing. You will manage day-to-day interactions with key government stakeholders, represent Moderna on the UKHSA operations board, and drive cross-functional collaboration to deliver on program objectives and commitments.

Moderna London, United Kingdom

On-site Permanent

Associate Director, Resilience Strategic Partnerships – UK

This role involves leading the execution of Moderna's strategic partnership with the UK government, focusing on mRNA-based vaccines and biomanufacturing. You will manage day-to-day interactions with key government stakeholders, represent Moderna on the UKHSA operations board, and drive cross-functional collaboration to deliver public health impact.

Moderna Tameside, SK15 3JG, United Kingdom

On-site Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.

GSK Stevenage, United Kingdom

Hybrid Permanent

Analytical Chemistry - Platform Modalities Leader

This role involves leading the strategic expansion and modernization of analytical chemistry platforms for complex therapeutic modalities, including small molecules, drug conjugates, and oligonucleotides. The Platform Modalities Leader will drive the adoption of new technologies, ensure robust and scalable analytical capabilities, and provide hands-on technical leadership while influencing cross-functional teams.

GSK Stevenage, United Kingdom

On-site Permanent

Head of RII or Oncology Programming

This senior leadership role involves overseeing the transformation of clinical data into regulatory-ready evidence for GSK's Respiratory, Immunology & Inflammation (RII) or Oncology Research Unit. The Head of RII or Oncology Programming will lead a global team, drive strategic initiatives, and champion innovation in clinical programming, ensuring high standards of quality, compliance, and timely delivery of medicines and vaccines.

GSK Stevenage, United Kingdom

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for global R&D trials, translating protocols into operational supply strategies, and ensuring on-time delivery of investigational products. The Clinical Trial Supply Manager acts as the key link between clinical teams and supply operations, overseeing demand planning, depot management, and compliance across Phase I–IV studies, including investigator-sponsored and compassionate use trials.

GSK Stevenage, United Kingdom €48,375 – €116,000 pa

On-site Permanent

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Global Study Lead to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.

GSK Stevenage, United Kingdom

Hybrid Permanent