The Discovery Disease Area Lead for Cardiovascular-Renal Diseases at GSK will lead the identification and validation of therapeutic targets for chronic kidney disease, glomerulonephritis, and cardiovascular conditions. You will manage a cross-functional team, drive scientific excellence, and collaborate with external experts to translate human disease phenotype information into actionable therapeutic innovations.
This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation and benefit-risk management across clinical development and post-marketing settings. The position requires expert analysis of clinical and safety data, leadership in cross-functional governance teams, and strategic input into regulatory submissions and risk mitigation. It plays a critical part in ensuring patient safety and regulatory compliance within immunology and other therapeutic areas.
This role involves servicing and repairing advanced medical diagnostic systems used in NHS laboratories and clinical chemistry environments. The engineer will visit customer sites to perform maintenance, troubleshoot issues, and deliver technical solutions while working closely with laboratory staff. The position requires a technically skilled individual with experience in high-value capital equipment and offers extensive product training.
Perform on-site installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratory settings. Provide technical troubleshooting and customer support across pathology and clinical chemistry environments. Receive full product training and work with cutting-edge diagnostic equipment from a global market leader.
This role leads global regulatory CMC strategy for mRNA-based medicines, developing and implementing regulatory plans for international submissions. The individual will guide CMC documentation, interact with health authorities, and provide strategic input across product development stages, ensuring compliance with EU and global regulations. The position plays a key part in advancing Moderna’s pipeline of transformative therapeutics across vaccines, oncology, and rare diseases.
This role involves leading CMC regulatory strategy for global mRNA product development, preparing and reviewing regulatory submissions, and guiding cross-functional teams on compliance and agency interactions. The position requires deep expertise in biologics CMC regulations, particularly in EU and ROW markets, and plays a key part in shaping regulatory pathways across vaccines, oncology, and rare diseases. Based at the Harwell site, it emphasizes in-office collaboration within a multidisciplinary team.
This role involves leading the end-to-end safety strategy for oncology programs, managing safety signals, and ensuring compliance with regulatory requirements. You will work closely with global teams, health authorities, and internal leaders to drive safety governance and benefit-risk evaluations.
Leads the technical architecture and development of a global medical insights platform, translating business and regional needs into scalable technical solutions. Drives innovation by evaluating new data sources, AI methods, and analytics approaches for integration. Works across engineering, data, and stakeholder teams to deliver a robust, evolving platform in a highly collaborative, matrixed environment.
Leads the technical architecture and development of Pfizer's global Medical Insights platform (InsightXplorer), translating regional and business needs into scalable technical solutions. Drives innovation by evaluating new data sources, AI methods, and analytics approaches for integration. Collaborates with cross-functional teams to ensure platform evolution aligns with medical and scientific objectives.
The Global Program Regulatory Director at Novartis leads the development and execution of global regulatory strategies for innovative medicines. Key responsibilities include guiding Health Authority interactions, evaluating regulatory risks, and leading cross-functional teams to drive successful product development and commercialization.
This role involves leading the end-to-end clinical supply chain strategy for global trials, managing demand forecasting, packaging, labeling, distribution, and inventory. You will work closely with cross-functional teams to ensure supply strategies align with trial milestones and commercial readiness, leveraging AI and advanced tools to optimize processes.
The Vice President, Medical Affairs, will lead the development and execution of integrated medical strategies for Recursion's clinical portfolio, focusing on areas like oncology, rare disease, and immunology. Key responsibilities include building evidence-generation plans, engaging with key opinion leaders, and ensuring compliance with medical and regulatory standards.
This role involves leading global clinical strategy for Roche’s toxicology and drug testing portfolio, including designing and executing high-impact clinical development programs. The Clinical Development Leader will drive regulatory interactions, integrate real-world evidence, and collaborate with key opinion leaders to advance diagnostic innovations. The position emphasizes scientific leadership, cross-functional collaboration, and mentoring within a globally distributed team.
Leads global clinical strategy for Roche’s toxicology and drug testing portfolio, designing and executing clinical development programs to support regulatory approval and market adoption. Acts as scientific authority in interactions with health agencies, drives real-world evidence integration, and collaborates with KOLs and cross-functional teams to advance diagnostic innovation. Focuses on generating robust clinical evidence to demonstrate safety, effectiveness, and scientific validity of diagnostic solutions.
This role involves leading the site's Quality Management System and regulatory compliance activities, ensuring alignment with ISO standards and regulatory requirements. You will manage audits, inspections, CAPAs, risk assessments, and continuous improvement initiatives, while also developing and mentoring quality professionals.
