This role involves leading clinical development for aging-related research within GSK’s Respiratory, Immunology & Inflammation unit. The Medical Director will design and execute clinical development plans, provide medical oversight, and integrate translational and clinical data to advance drug candidates. The position emphasizes cross-functional leadership, regulatory engagement, and innovation in addressing unmet needs in aging and immune science.
This role involves leading clinical development for aging-related therapies within GSK’s Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and execute clinical development plans, provide medical oversight, and integrate translational and clinical data to advance drug candidates. The position emphasizes cross-functional leadership, regulatory engagement, and innovation in trial design to deliver differentiated medicines.
This role involves designing and conducting experiments in advanced genome technologies and next-generation plant transformation to enhance plant engineering capabilities. The scientist will work on genetic manipulation, DNA/RNA delivery, and plant regeneration, contributing to high-impact research with real-world applications in food security and sustainable agriculture. Collaboration with AI, automation, and generative biology experts across EIT’s ecosystem is a key part of the role.
The Controlled Environment Lead will build and oversee plant growth and phenotyping facilities, ensuring controlled and reproducible environments for high-impact plant science research. Responsibilities include hands-on cultivation, data collection, and leading the team to support scientific and commercial goals.
The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.
The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.
This role involves servicing, installing, repairing, and calibrating sophisticated scientific and laboratory systems used in pharmaceutical and research environments. You will work with high-value capital equipment, providing technical support and customer service.
This role involves servicing, installing, repairing, and calibrating sophisticated scientific and laboratory systems used in pharmaceutical and research environments. The position requires a background in field service engineering, particularly with high-value capital equipment and electronics.
This role involves managing and reporting on complex scientific projects, particularly two Innovate UK-funded projects, at a biotechnology company. Responsibilities include project planning, financial tracking, risk management, and coordinating with scientific teams and external partners. The position offers the opportunity to improve project management processes and support future grant applications.
This role involves leading the delivery of the Sector Operating Plan, managing tenant and investor relationships, and supporting founders and portfolio companies at ONE BioHub in Aberdeen. You will also plan and deliver sector events, monitor budgets, and support governance processes.
This role involves managing the day-to-day operations of a life sciences facility, including laboratory and office space, ensuring compliance with health and safety standards, and supporting tenants. The manager will also handle leasing, facility maintenance, and technical services, contributing to the facility's growth and development.
Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.
This role involves deploying and adapting proprietary generative AI models within pharmaceutical and biotech customer environments. You'll work closely with interdisciplinary teams to integrate models into production systems, optimize performance, and translate scientific requirements into technical solutions. The position requires deep expertise in generative modelling, strong ML engineering skills, and the ability to act as a technical liaison between research and customer teams.
