Experteer Overview
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In this Senior CRA I role, you monitor oncology trials to ensure ICH-GCP compliance and data integrity across sites. You will work on-site or remotely, partnering with cross-functional teams to manage site performance, safety, and regulatory adherence. The position offers opportunities to mentor junior CRAs, lead site interactions, and contribute to RWLP studies. You join a client-focused organization that values agility, collaboration, and delivering meaningful patient outcomes. This is a chance to shape trial execution at scale within a global sponsor environment.
Compensaciones / Beneficios
• Perform site qualification, initiation, monitoring, management, and close-out visits ensuring regulatory and protocol compliance.
• Assess site performance, escalate issues, and develop action plans with project teams.
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