Clinical Project Lead (Continuous Glucose Monitoring) — Roche
NewCHF 85'500 - 129'500
Roche · Basel (BS)
- Location
- Basel
- Contract
- full-time
- Posted
- Yesterday
SalaryCHF 85'500 - 129'500
Role overview
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.
- 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.
- Key Responsibilities :
- Lead and oversee the global study team, ensuring full accountability for study deliverables including quality, budget, and timelines.
- Strong experience in clinical trial management, particularly in the Continuous Glucose Monitoring field
- You have a degree in Life Sciences, Healthcare, or a related field. A background in multiple disease areas is a plus.
Main responsibilities
- 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.
Key requirements
- Strong experience in clinical trial management, particularly in the Continuous Glucose Monitoring field
- 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 man
Additional details
- Join Roche, where every voice matters.
- You have a degree in Life Sciences, Healthcare, or a related field. A background in multiple disease areas is a plus.
Notes and original content
- The Position
- Your Profile :
- You have a degree in Life Sciences, Healthcare, or a related field.
- A background in multiple disease areas is a plus.
