Experteer Overview
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In this role you drive site monitoring and management for multicenter trials within a hybrid, multisponsor setup. You collaborate with site teams to ensure regulatory, ICH-GCP and study protocol adherence while safeguarding data integrity and subject safety. You will manage site qualification, initiation, monitoring, IP handling, and documentation, and support trial readiness and team collaboration. The position offers impact across real-world late-phase studies and global study teams, with a chance to shape monitoring processes and improve trial outcomes.
Compensaciones / Beneficios
• Perform site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote) with regulatory and protocol compliance
• Verify informed consent and protect subject confidentiality; assess safety and data i...