Associate, Study Management II//CTM II

📋 Description

• Responsible for executing one or more elements of clinical studies in compliance with quality
• Supports the Study Project Manager in leading the cross-functional study team, including
• Responsible for regular updates to the cross-functional team and stakeholders on study status
• Supports the development of the clinical study blueprint/protocol and associated systems and
• Supports vendor selection, scope development, management and oversight of external vendors in
• Responsible for generating study-related training for the study team, study sites, and vendors for

🎯 Requirements

• Bachelor's Degree or OUS equivalent degree required, typically in nursing or scientific field
• Two years of Pharma-related/clinical research related experience or professional equivalent desired.
• Demonstrates analytical and critical thinking skills.
• Possesses good communication skills.