Lead clinical pharmacology, modeling, and simulation efforts for infectious disease assets, driving dose selection and development strategy through population PK/PD and exposure-response modeling. Serve as a scientific leader within cross-functional teams while remaining hands-on with quantitative analyses. Contribute to regulatory submissions and advance model-informed drug development across the R&D lifecycle.
Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying quantitative methods to inform dose selection, trial design, and regulatory strategy. Work across development phases from early planning to lifecycle management, using population PK/PD and exposure-response modelling. Operate as a scientific leader within a cross-functional environment while remaining hands-on with data analysis and model development.
This role leads the execution and delivery of AI initiatives within Global Clinical Operations, translating innovative concepts into scalable, compliant solutions. The Associate Director will coordinate cross-functional teams, manage the AI product roadmap, and drive adoption of AI tools across clinical trial operations. It involves strong program management, change leadership, and collaboration with technology and clinical stakeholders to transform how AI enhances productivity and compliance in drug development.
This role involves providing strategic medical leadership for Novartis' Immunology portfolio in the UK, shaping local medical strategy in alignment with global priorities. The Medical Lead will drive scientific engagement, lead evidence generation including real-world studies, and translate insights into actionable plans across cross-functional teams. Key responsibilities include leading medical education initiatives, supporting product launches, and fostering relationships with key external stakeholders such as medical experts and patient organisations.
This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountability point for global regulatory submissions. The individual will direct cross-functional teams in designing and executing Phase 1-3 trials, develop clinical development plans, and contribute to regulatory filings, safety reports, and product labeling. The position emphasizes leadership in obesity-related therapeutics, digital innovation in clinical development, and engagement with external scientific and regulatory stakeholders.
This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity and chronic weight management. The Global Development Lead is responsible for end-to-end clinical strategy, including designing and executing global clinical trials, regulatory submissions, and cross-functional team leadership. The position requires deep therapeutic expertise, strategic input into product development, and engagement with external stakeholders such as advisory boards and regulatory bodies.
This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials, ensuring patient safety and clinical integrity. The Medical Director provides physician-level input into study design, data interpretation, and regulatory interactions, working closely with cross-functional teams and external experts. It emphasizes integration of medical expertise across clinical development, with a focus on advancing cancer treatments through innovative science and collaboration.
This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials within GSK’s global development programme. The Medical Director provides physician-level expertise in study design, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity across phases I–III. Working within a cross-functional matrix team, the role integrates medical insight into clinical strategy and collaborates with external experts and investigators to advance innovative cancer therapies.
Lead clinical pharmacology modeling and simulation efforts for infectious disease assets, combining hands-on pharmacometric analysis with strategic input across clinical development. Design and interpret studies, develop population PK/PD models, and guide dose selection and regulatory strategies. Work within cross-functional teams to influence development decisions and advance model-informed drug development.
Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying pharmacokinetic/pharmacodynamic and population modelling to inform dose selection, trial design, and regulatory strategy. This senior individual contributor role combines hands-on quantitative analysis with strategic leadership across development phases, from early planning to lifecycle management. Work within a science-driven team to advance model-informed drug development using tools like NONMEM, R, and PBPK, while collaborating with cross-functional partners and supporting regulatory submissions.
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.
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.
Leads end-to-end delivery of clinical study portfolios for a specific asset, coordinating proposal reviews for investigator-initiated and collaborative studies. Manages milestone tracking, budget forecasting, supply coordination, and stakeholder communication across cross-functional teams. Acts as primary operational contact and provides oversight in compliance with GCP and regulatory standards, while supporting team development and process improvements.
This role involves leading AI-first product development for clinical trial site management systems at GSK, focusing on transforming how trials are conducted through intelligent automation and data-driven decision-making. The Product Owner will own the strategy and delivery of scalable digital capabilities across feasibility, study start-up, contracting, and monitoring, ensuring adoption and compliance in a regulated GxP environment. Key responsibilities include driving innovation with AI-native solutions, aligning stakeholders, and embedding transformative technology into core operational workflows.
Author and lead the development of high-quality clinical regulatory documents such as protocols, Clinical Study Reports, and CTD submissions. Interpret complex clinical and statistical data to produce accurate, compliant narratives. Collaborate with cross-functional teams and manage complex writing projects across therapeutic areas and global submissions.
