Found Description
Experteer Overview
Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia. Si su perfil encaja, presente su candidatura.
As a Global Study Associate, you support global clinical study delivery within Clinical Operations by coordinating study setup through close-out. You work with GSD, GSAD, and GSM to ensure quality, compliance, and timely execution across multiple studies. You manage eTMF setup and maintenance, regulatory document handling, and administrative processes with cross-functional and external stakeholders. This role offers hands-on exposure to study administration, regulatory submissions, and process improvements that drive study success and compliance.
Compensaciones / Beneficios
• Set up and maintain the electronic Trial Master File (eTMF) and oversee its close-out for ICH/GCP compliance
• Coordinate regulatory document collection and ensure templates and versions align with study requirements
• Sup...
Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia. Si su perfil encaja, presente su candidatura.
As a Global Study Associate, you support global clinical study delivery within Clinical Operations by coordinating study setup through close-out. You work with GSD, GSAD, and GSM to ensure quality, compliance, and timely execution across multiple studies. You manage eTMF setup and maintenance, regulatory document handling, and administrative processes with cross-functional and external stakeholders. This role offers hands-on exposure to study administration, regulatory submissions, and process improvements that drive study success and compliance.
Compensaciones / Beneficios
• Set up and maintain the electronic Trial Master File (eTMF) and oversee its close-out for ICH/GCP compliance
• Coordinate regulatory document collection and ensure templates and versions align with study requirements
• Sup...