Global Study Lead — 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.
- The Global Study Lead is responsible for ensuring that all studies are designed, planned, executed, monitored, closed out and documented in an appropriate manner within the planned timeframe and cost; ensuring that the sponsor responsibilities are fulfilled, while assuring compliance to all applicable regulatory requirements.
- Responsible for the timeline and budget planning and execution of studies.
Main responsibilities
- The Global Study Lead is responsible for ensuring that all studies are designed, planned, executed, monitored, closed out and documented in an appropriate manner within the planned timeframe and cost; ensuring that the sponsor responsibilities are fulfilled, while assuring compliance to all applicable regulatory requirements.
- Responsible for the timeline and budget planning and execution of studies.
- Assigns and ensures delivery of specific tasks to/from other members of the study team.
- Provides oversight to outside support including CROs, consultants and/or medical advisors The Opportunity:
- The key accountabilities for this position include, but are not limited to:
- Leads the global study team with full accountability for the study deliverables with respect to quality, budget and timelines, in collaboration with the Study Team and ensures the development of high quality study designs for sponsored studies in collaboration with internal and external experts
- In collaboration with Program Leadership, prepares different scenarios for evidence generation (e.g. study, real-world evidence) in cross-functional collaboration (e.g. with Regulatory Affairs, R&D, CDMA Project Teams) to support global strategies and planning of timeline and costs
- Develops key study documents (i.e., Design Validation Plan, protocol, study training materials, study forms and templates, study report)
- Oversees planning and operational aspects of companion diagnostics studies sponsored by Pharma partners
- Accountable for study-level budget of assigned studies.
Additional details
- Join Roche, where every voice matters. A healthier future.
- Provides oversight to outside support including CROs, consultants and/or medical advisors
- Build and maintain strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders and other alliance partners, including CROs, in meeting business goals and ensuring operational excellence.
Notes and original content
- Join Roche, where every voice matters.
- The Position
- A healthier future.
- The Opportunity:
- Who you are:
