Global Study Lead (Near Patient Point of Care, Cardiovascular & Metabolic Diseases)

## Global Study Lead (Near Patient Point of Care, Cardiovascular & Metabolic Diseases)Candidatar-selocations: Motherwell: Burgess Hill: Viennatime type: Tempo integralposted on: Publicado hojetime left to apply: Data de término: 14 de junho de 2026 (19 dias restantes para se candidatar)job requisition id: 202605-112209Na Roche, você pode-se apresentar como você mesmo, abraçado pelas qualidades únicas que traz. Nossa cultura incentiva a expressão pessoal, o diálogo aberto e as conexões genuínas, onde você é valorizado e respeitado por quem você é, e permitindo que você prospere tanto pessoal como profissionalmente. É assim que pretendemos prevenir, deter e curar doenças e garantir que todos tenham acesso aos cuidados de saúde hoje e nas gerações futuras. Junte-se à Roche, onde cada voz é importante.### A posiçãoAt **Roche Diagnostics Solutions (RDS),** our mission is clear: to diagnose earlier, develop faster, and personalise treatment because every patient is unique. Our **Clinical Development & Medical Affairs (CDMA)** team drives innovation to improve healthcare outcomes globally.We see ourselves and our customers as a team that can only reach its full potential together. By listening closely to patients and physicians, and leveraging digitalisation and new technologies, we get closer to their real-world needs. This collaborative spirit creates an environment where ideas can grow and new ways of doing things can be tried – resulting in competitive products that get to patients faster.Our work spans the entire product lifecycle, from discovery to post-launch. By collaborating with internal teams, external partners, and patients, the CDMA chapter provides crucial medical insights, designs and executes clinical studies, and offers on-market support. Ultimately, we generate the comprehensive clinical evidence that demonstrates product safety, effectiveness, and scientific validity – facilitating smooth product registration, adoption and reimbursement globally so we can save lives and improve patient quality of life.We are looking for a dynamic and experienced **Global Study Lead** to join our team. In this pivotal role, you will lead global study teams to ensure the successful execution of clinical studies. You will be responsible for delivering high-quality study designs, adhering to timelines and budgets, and collaborating with cross-functional teams to support evidence generation strategies. If you have a passion for advancing clinical trials in the cardiovascular/metabolic area, specifically in Near Patient Care , we would love to hear from you!**Key Responsibilities**:* Lead and oversee the global study team, ensuring full accountability for study deliverables including quality, budget, and timelines.* Collaborate with Program Leadership to prepare different scenarios for evidence generation (e.g., study, real-world evidence) and ensure cross-functional cooperation with Regulatory Affairs, R&D, Biostatistics, Data Management, Medical Affairs and CDMA Project Teams.* Develop key study documents such as Design Validation Plans, study protocols, training materials, study forms, templates, and study reports.* Maintain responsibility for the study-level budget of assigned studies.* Ensure compliance with regulations, guidelines, and standard operating procedures, while ensuring audit/inspection readiness.* Oversee execution of sponsored studies for registrational and non-registrational purposes through all study phases (planning, start-up, conduct, and close-out).* Manage study activities outsourced to service providers, including CROs, ensuring timely and quality execution.* Work with the Publication Team to ensure study results are effectively published.* Track project performance and ensure that projects are completed on time, within scope, and within budget.* Build and maintain strong, collaborative relationships with internal and external stakeholders, including cross-functional teams, CROs, opinion leaders, investigators, and key customers.**Your Profile:*** Strong experience in clinical trial management, particularly in the cardiovascular/metabolic indication and Near Patient Care or Point of Care. Experience with studies in an emergency department setting is a plus.* You have a degree in Life Sciences, Healthcare, or a related field. A background in multiple disease areas is a plus.* You have practical knowledge of clinical trial management and product development, with a solid understanding of Clinical Operations.* Ability to lead and manage projects and provide guidance to less experienced colleagues.* Strong analytical skills to solve complex problems and provide innovative solutions.* You’re able to explain difficult or sensitive information and build consensus among stakeholders.* You have a proven ability to build and maintain relationships with internal teams, external partners, and key stakeholders, including CROs and international opinion leaders.If you’re looking to make a significant impact in a leading global healthcare organisation and have the required experience and qualifications, we invite you to apply today. Please upload only your current compelling CV and / or Cover Letter. We look forward to receiving your application!#J-18808-Ljbffr…