CRA II in Romania
Core
Clinical Research Associate (Level II) performing risk-based monitoring, site management, and data verification for clinical trials.
Role type
Clinical Research Associate (Level II)
Builds
Clinical trial data and compliance
Domain
Clinical Research / Life Sciences
Required skills
Risk-based monitoring, Root cause analysis, Protocol compliance, ICH-GCP guidelines, Site initiation, Data verification (SDR/SDV/CRF), Investigational product inventory, Trial close-out
Preferred skills
Medical/therapeutic area knowledge, Clinical Trial Management Systems (CTMS)
Technologies
Microsoft Office, Clinical Trial Management Systems (CTMS)
Responsibilities
Monitor investigator sites with a risk-based approach, Conduct on-site and remote monitoring visits, Ensure data accuracy through document review, Initiate and close out clinical trial sites, Manage investigator payments and documentation, Facilitate communication between sites and project teams
Seniority
Mid-level, hands-on IC
