Global Study Lead

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.

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!

• 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, 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.

• Strong experience in clinical trial management, particularly in the cardiovascular/metabolic indication and Near Patient 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.
• You are able to be onsite at our Scotland, LumiraDx site, Stirling roughly 2-3 days per week.

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!

Roche is an Equal Opportunity Employer.