Latest IT Recruitment Jobs

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Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents such as protocols, Clinical Study Reports, and submission dossiers for global regulatory agencies. The Principal Medical Writer will lead complex writing projects, collaborate with cross-functional teams, and translate clinical and statistical data into clear, compliant narratives. The position emphasizes leadership in document strategy, regulatory interpretation, and the use of automation tools within a hybrid work environment.

GSK Stevenage, United Kingdom CA$118,000 – CA$168,000 pa
Hybrid Permanent
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Engineering Technician (numerous vacancies)

This role involves providing engineering support across manufacturing operations at GSK’s Ware site, performing electrical and mechanical maintenance, calibration, fault diagnosis, and continuous improvement activities on production and utilities equipment. Technicians work in regulated GMP environments across respiratory, oral solid dose, or facilities teams, ensuring compliance with safety and quality standards. The role includes shift work and collaboration with cross-functional teams to maintain high-throughput pharmaceutical manufacturing.

GSK East Hertfordshire, United Kingdom
On-site Permanent Shift-work

Clinical Data Strategy, Manager

This role involves leading clinical data strategy planning and execution across Translational Medicine programs, with a focus on designing fit-for-purpose data collection approaches and supporting robust decision-making. The individual will develop Data Strategy Plans, guide trial teams on data oversight, and leverage internal and external data to inform trial design—particularly in Neuroscience. The position requires deep expertise in clinical assessments, data integrity, and cross-functional collaboration in a global, fast-paced environment.

Novartis London, United Kingdom £49,140 – £91,260 pa
Hybrid Permanent

Senior Principal Developer

Develop and maintain R packages and Shiny applications to support clinical trial data analysis and reporting workflows. Collaborate with statisticians and programmers to build reproducible, AI-enhanced tools, with a focus on open-source practices and modernization. Support user experience improvements and drive adoption through training and documentation.

Novartis £57,050 – £105,950 pa
Remote Permanent
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Global Development Lead, Internal Medicine, Sr. Director (MD)

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountable leader for global drug development programs. The position involves end-to-end responsibility for clinical strategy, trial design, regulatory submissions, and cross-functional team leadership across a complex matrix environment. It also includes engagement with external stakeholders, patient advocacy groups, and oversight of safety and lifecycle planning, with a focus on obesity and related therapeutic areas.

Pfizer £274,500 – £457,500 pa
On-site Permanent
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Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for internal medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapeutics. The Global Development Lead serves as the primary clinical accountability point, designing and executing global clinical development plans, regulatory submissions, and cross-functional team leadership. The position requires deep expertise in endocrinology or chronic weight management and extensive experience in Phase 1-3 clinical trials, translational medicine, and regulatory strategy across global markets.

Pfizer United States £214,900 – £358,100 pa
On-site Permanent
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Senior Medical Director, Oncology Clinical Development - Sarcoma

This role involves leading clinical development for sarcoma within GSK's oncology portfolio, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and represent the programme externally at scientific forums. Based on-site in Waltham, MA, the position requires integration with cross-functional teams and mentorship of clinical staff to ensure patient-centred, scientifically rigorous drug development.

GSK £284,250 – £473,750 pa
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Director, Clinical Operations Asset Lead

Leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, timely delivery of clinical studies. Works closely with cross-functional teams to align execution with scientific and regulatory goals, while managing risks, vendors, and stakeholder engagement. Focuses on patient-centric innovation and inspection readiness within a global biopharma environment.

GSK US$189,750 – US$316,250 pa
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Director, Clinical Operations Asset Lead

Leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to align study design with strategic goals, manage vendor and resourcing strategy, and maintain inspection readiness. Serves as the primary escalation point for operational and quality issues, driving governance and risk management.

GSK
Hybrid Permanent
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Director, Clinical Operations Asset Lead

Leads clinical operations for a key asset across its full lifecycle, ensuring operational strategy aligns with scientific and regulatory goals. Drives study execution, vendor and resourcing strategy, and cross-functional coordination to deliver high-quality clinical data. Focuses on innovation, risk management, and inspection readiness within a global, matrixed environment.

GSK
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Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and execute model-informed drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize clinical trial design, dose selection, and regulatory submissions. Drive innovation in quantitative clinical pharmacology across the R&D pipeline, from early development through lifecycle management, within a multidisciplinary translational medicine team.

GSK £119,250 – £198,750 pa
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Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and deliver model-informed drug development (MIDD) strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize clinical trial design, dose selection, and regulatory submissions. Work across multidisciplinary teams to advance GSK’s oncology pipeline using quantitative approaches including exposure-response modeling, disease progression models, and simulation-based trial design. Drive innovation through external collaborations, publications, and adoption of cutting-edge methodologies in clinical pharmacology.

GSK
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Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and execute model-based drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize dose selection, trial design, and regulatory submissions. Drive innovation in clinical pharmacology through cross-functional collaboration and external engagement. Operate in a science-driven environment focused on accelerating the development of novel cancer therapies.

GSK US$188,100 – US$313,500 pa
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Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead clinical pharmacology and modelling & simulation efforts for oncology drug development, applying AI/ML and quantitative methods to optimise dosing, trial design, and regulatory strategy. Drive innovation in model-informed drug development across small molecules, biologics, and antibody-drug conjugates. Collaborate with cross-functional teams to accelerate therapies to patients using advanced pharmacometric and machine learning techniques.

GSK £188,100 – £313,500 pa
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Senior Medical Director, Oncology Clinical Development - Sarcoma

This role involves leading clinical development in oncology with a focus on sarcoma, providing medical oversight and strategic input across study design, execution, and data interpretation. The position ensures patient safety and clinical integrity while guiding cross-functional teams and engaging with external experts. It requires deep expertise in oncology drug development and strong leadership in a matrixed global environment.

GSK US$284,250 – US$473,750 pa