This role involves leading medical oversight in oncology clinical development, focusing on hematology and clonal myeloid disorders. The Medical Director will guide study design, ensure patient safety, interpret clinical data, and collaborate with cross-functional teams and external experts. It is a physician-led position embedded in clinical strategy with a strong emphasis on real-world impact and regulatory engagement.
This role involves providing medical leadership in oncology clinical development, with responsibilities spanning study design, medical monitoring, safety oversight, and data interpretation. The Medical Director will integrate physician-level insights into clinical trials, collaborate with cross-functional teams and external experts, and contribute to regulatory submissions and scientific communications. The position emphasizes patient-centered decision-making and real-world impact in cancer treatment innovation.
This role involves leading the creation and management of investigator site budgets and contracts for clinical trials, using Grants Manager and FMV benchmarking tools. The candidate will oversee CRO activities, ensure budget consistency across trials, and support timely site activation by managing negotiations and identifying risks. Collaboration with legal, clinical operations, and external partners is central to ensuring compliance and efficiency in contract execution.
Lead the development and validation of molecular assays including RT-qPCR, dPCR, and NGS for clinical biomarker programs across Moderna's therapeutic pipeline. Drive end-to-end assay lifecycle management, ensure regulatory compliance with GCLP standards, and collaborate with cross-functional teams to deliver high-quality genomic data. Mentor scientists and integrate advanced analytics and AI-enabled tools to accelerate discovery and translational research.
This role leads the end-to-end sample-to-sequence pipeline for the Trillion Gene Atlas, managing high-throughput DNA processing from extraction through to sequencing dispatch. The individual will translate R&D protocols into scalable production workflows, drive continuous operational improvements using Lean/Six Sigma, and lead a team within a fast-paced, interdisciplinary environment. They will also evaluate and integrate emerging sequencing technologies and automation to scale throughput and reliability.
This role involves operating and maintaining equipment in a cGMP-regulated mRNA vaccine production environment, ensuring safe and compliant manufacturing processes. The associate will execute production operations, support quality assurance, troubleshoot technical issues, and contribute to continuous improvement initiatives. Work is conducted in a highly automated, digitally enabled facility with a focus on operational excellence and innovation in mRNA technology.
This two-year graduate programme at GSK focuses on engineering and manufacturing, with rotations in various areas like project management, equipment reliability, and smart manufacturing. Participants will work on real-world challenges, apply digital and data analytics, and contribute to sustainability initiatives.
This two-year graduate programme at GSK's Ware site focuses on quality science in pharmaceutical manufacturing. Participants will gain hands-on experience in quality testing, regulatory compliance, and sustainability projects, while developing skills in data analytics and continuous improvement.
This two-year graduate programme at GSK focuses on engineering and manufacturing in the pharmaceutical industry. Participants will work on real manufacturing challenges, manage equipment, implement smart manufacturing technologies, and contribute to sustainability initiatives. The role involves cross-functional projects, rotations, and tailored training to develop technical and leadership skills.
This two-year Supply Chain Graduate Programme at GSK in Barnard Castle focuses on manufacturing and supplying medicines and vaccines. Participants will work on cross-functional projects, gain exposure to external manufacturing, and develop skills in digital data and analytics, sustainability, and project management.
This two-year graduate programme at GSK focuses on quality science in pharmaceutical manufacturing. Participants will gain hands-on experience in quality testing laboratories and manufacturing facilities, working on regulatory compliance, quality systems, and sustainability projects. The role involves cross-functional collaboration and training in advanced problem-solving techniques.
Leads clinical development for vascular programmes across early and late phases, shaping study designs and clinical development plans. Works cross-functionally with translational science, regulatory, and commercial teams to advance medicines for vascular disease, with a focus on patient impact and scientific innovation. Provides medical oversight, contributes to regulatory submissions, and guides decision-making in a matrix environment.
This role involves providing technical leadership for facility and utility systems at Moderna’s new biotech site in Harwell, Oxford. The Facilities Engineering Manager will oversee maintenance, vendor performance, and engineering projects across R&D and manufacturing environments, ensuring compliance and operational reliability. The position emphasizes continuous improvement, digital tool integration, and collaboration with global teams in a GMP-regulated setting.
This role involves providing medical and scientific leadership in safety evaluation and risk management for GSK’s clinical and post-marketing assets. The Associate Medical Director will lead safety strategy, contribute to regulatory submissions, and guide cross-functional teams in pharmacovigilance activities. The position emphasizes evidence-based decision-making, global regulatory compliance, and proactive risk communication within a matrix environment.
This role involves providing medical and scientific leadership in safety evaluation and risk management for GSK's clinical and post-marketing assets. The Associate Medical Director will lead signal detection, contribute to pharmacovigilance strategy, and ensure robust safety oversight across global development programs. Working within a cross-functional matrix, the role emphasizes evidence-based decision-making, regulatory compliance, and proactive risk communication to protect patient safety.
