Cra I
Core
Overseeing and coordinating clinical trials, ensuring regulatory compliance, and collecting and analyzing critical data for clinical development.
Role type
Clinical Research Associate (CRA)
Builds
Clinical studies and trial data
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Knowledge of ICH-GCP guidelines, ability to review and evaluate medical data, study coordination, query management, feasibility study preparation
Preferred skills
Ability to travel 60% of the time (international and domestic), valid driver's license
Technologies
None stated
Responsibilities
Coordinate all activities for setting up and monitoring a study, complete accurate study status reports, maintain study documentation, run sponsor generated queries efficiently, prepare and review study documentation and feasibility studies for new proposals, ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements
Seniority
Entry-level (CRA I)