Possesses advanced computer skills, good verbal and written communication skills, and strong
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 preparing
Supports the development of clinical study blueprint/protocol and associated systems and documents
Supports vendor selection, scope development, management and oversight of external vendors in
Generates study-related training for study team, study sites, and vendors

🎯 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

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