This role involves developing and executing the analytical network strategy for GSK's supply chain, ensuring alignment with quality objectives. Responsibilities include defining QC testing principles, driving innovation in QC testing, and collaborating with cross-functional teams to integrate analytical testing into the end-to-end supply chain process.
This role involves developing and executing the analytical network strategy for GSK's supply chain, ensuring alignment with quality objectives. Responsibilities include defining QC testing principles, driving innovation in QC testing, and collaborating with cross-functional teams to integrate analytical testing into the end-to-end supply chain process.
As Lead Central Monitor, you will lead a team of Central Monitors, shaping monitoring strategies to ensure patient safety and data integrity in clinical trials. You will work across clinical, data, and risk-surveillance teams to translate complex risk signals into actionable insights and drive continuous improvement through analytics and technology.
As Lead Central Monitor, you will lead a team of Central Monitors, shape monitoring strategies, and ensure data integrity and patient safety in clinical trials. You will work across clinical, data, and risk-surveillance teams to translate complex risk signals into actionable insights and drive continuous improvement through analytics and technology.
This role involves servicing, installing, repairing, and calibrating sophisticated medical laboratory automation systems across Europe. You will support scientific products in various settings, including pathology departments, university research labs, and pharmaceutical environments, with extensive travel and frequent overnight stays.
This role involves servicing, installing, repairing, and calibrating sophisticated medical laboratory automation systems across Europe. You will work with a variety of scientific products in pathology departments, research labs, and pharmaceutical environments, requiring extensive travel and frequent overnight stays.
This role involves leading regulatory strategy and hands-on activities for medicinal products, medical devices, and cosmetics in the UK and Ireland. Responsibilities include managing regulatory submissions, ensuring compliance, and supporting product launches and lifecycle management.
This role involves managing the security, storage, and retrieval of proprietary and client information, using scanning equipment and maintaining accurate records. The position also includes developing and implementing a sustainability strategy for IQVIA Laboratories and providing reference services to internal clients.
The Global Research Program Manager will drive internal operational efficiency, coordinate cross-team projects, manage key partnerships, and oversee the tools and operations that the technical teams rely on. This role involves optimizing processes, facilitating collaboration, and ensuring that the team can focus on pioneering research and development.
The QA Engineer will design, build, and maintain automated test frameworks using Java, Selenium, and RestAssured, ensuring high-quality software delivery. They will work closely with Agile teams to improve test coverage, automate testing, and support continuous integration and delivery processes.
Lead translational strategies for oncology and immunology programs by designing in vivo pharmacology and PK/PD studies to validate AI-designed drug candidates. Bridge computational predictions with experimental validation through CRO partnerships and biomarker-driven approaches. Drive preclinical data generation to inform clinical trial design and regulatory filings.
This role involves working in Pfizer's Regulatory Strategy department, contributing to the development and implementation of regulatory strategies for innovative medicinal products. Responsibilities include compiling regulatory documents, engaging with health authorities, and maintaining systems and processes. The position offers a unique overview of the pharmaceutical product life cycle from research to market.
This role involves designing and executing biological screening cascades to validate computational predictions in drug discovery. The scientist will lead biophysical, biochemical, and cellular assay development, collaborate with CROs, and bridge AI-driven insights with experimental validation across oncology and immunology programs. Close collaboration with medicinal chemistry, structural biology, and machine learning teams ensures data informs rational drug design.
This role involves developing machine learning models grounded in quantum chemistry to accelerate small-molecule drug discovery. The scientist will create synthetic datasets using quantum mechanical methods, build scalable and reproducible ML pipelines, and collaborate with computational and experimental teams to model molecular energetics and protein–ligand interactions. Work contributes directly to drug design tools at Roche, with opportunities for scientific publication and open-source contributions.
Develop machine learning models grounded in quantum chemistry to accelerate small-molecule drug discovery. Create synthetic datasets using quantum mechanics and build scalable, deployable pipelines integrated into molecular design tools. Collaborate with computational and experimental scientists to advance drug discovery through publications and open-source contributions.
