Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.
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 technical leadership for facility and utility systems at Moderna’s biotech manufacturing site in Harwell. The Facilities Engineering Manager ensures operational reliability, oversees vendor performance, and drives maintenance excellence across R&D and manufacturing environments. The position emphasizes continuous improvement, compliance, and the use of digital tools including AI-enabled systems, within a GMP-regulated setting.
The Product Director, DevOps & CMO Performance role at GSK involves leading the development and delivery of Mission Control, a flagship AI-driven platform for optimizing clinical trial operations. Responsibilities include setting the technical roadmap, managing AI applications, ensuring compliance, and leading a multi-vendor delivery ecosystem.
The Medical Director, Oncology Clinical Development, focuses on lung and head/neck cancers, providing medical expertise and clinical judgement to design, conduct, and interpret clinical studies. Key responsibilities include medical monitoring, safety oversight, and collaborating with cross-functional teams to ensure patient safety and clinical integrity.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, protocol development, and collaboration with cross-functional teams and external experts.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. This role involves leading medical monitoring, ensuring patient safety, and collaborating with cross-functional teams to integrate medical considerations into study execution and regulatory interactions.
The Medical Director, Oncology Clinical Development role involves leading medical monitoring, safety oversight, and clinical data interpretation for clinical studies in lung and head/neck cancers. The role requires strong clinical expertise, collaboration with cross-functional teams, and engagement with external experts to ensure patient safety and study integrity.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, and collaboration with cross-functional teams to ensure patient safety and clinical integrity.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, and collaboration with cross-functional teams to ensure patient safety and clinical integrity.
This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will work in cross-functional teams, represent CMC in regulatory interactions, and mentor colleagues.
This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will work in cross-functional teams, represent CMC in regulatory interactions, and mentor colleagues.
This role involves leading the clinical development strategy for GSK's Hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific approaches, managing cross-functional teams, and ensuring regulatory compliance. The role requires extensive experience in oncology clinical development and leadership.
This role involves leading the clinical development strategy for GSK's Hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific approaches, managing cross-functional teams, and ensuring regulatory compliance. The role emphasizes innovation, collaboration, and patient-centric focus.
This role involves leading the clinical development strategy for GSK's hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific approaches, managing cross-functional teams, and ensuring regulatory compliance. The role emphasizes innovation, patient-centric focus, and strong leadership.
