Clinical Trial Coordinator
Core
Coordinate clinical trial activities, manage documentation in eTMF, support site activation, and ensure regulatory compliance for clinical studies.
Role type
Clinical Trial Coordinator (Administrative & Documentation)
Builds
Clinical trial study files, Investigator Site Files, regulatory submissions, and study documentation.
Domain
Clinical Research / Life Sciences
Required skills
Organizational skills, attention to detail, project management, data analysis, communication, computer proficiency (MS Office), risk identification
Preferred skills
Knowledge of ICH-GCP, Italian and European regulations, clinical research procedures, ability to work in international teams
Technologies
eTMF, Activate, clinical trial databases
Responsibilities
Coordinate assigned clinical trial activities, perform country and investigator file reviews, process and maintain clinical trial documentation, support site activation and regulatory submissions, liaise with internal teams and external sites, assist with study-specific translations
Seniority
Entry-level to Mid-level, hands-on IC
