Experteer Overview In this Global Study Lead role, you will drive the design and execution of worldwide clinical studies to generate high-quality evidence. You will work with cross-functional teams within Roche CDMA to translate scientific innovation into real-world patient impact. You’ll shape evidence strategies, lead study design, and ensure compliance and readiness across the study lifecycle. This position offers the opportunity to influence global clinical programs, partner with external investigators and CROs, and help accelerate access to innovative therapies.Compensaciones / Beneficios
- Direct global study teams and manage deliverables within quality, budget, and timelines
- Collaborate to develop evidence-generation scenarios including real-world evidence
- Develop study protocols, validation plans, and essential study documentation
- Foster relationships with internal experts, pharma partners, and international investigators
- Oversee outsourced activities and manage CROs and consultants
- Ensure readiness for global standards and audits, including ICH-GCP complianceResponsabilidades
- Experience in Clinical Operations or Product Development within the Healthcare industry with a track record of leading complex projects
- Bachelor in Life Sciences (advanced degree a plus)
- Strategic thinker with stakeholder negotiation and clear communication across audiences
- Solid understanding of international standards and regulations (IVDR, MDR, FDA) and their application in clinical studies
- Cultural awareness across time zones and diverse teamsRequisitos principales
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