CRA2 - FSP | Argentina
Core
Conducting clinical trial site selection, initiation, monitoring, and close-out visits while managing study documentation and quality.
Role type
Clinical Research Associate (monitoring)
Builds
Clinical trial data and regulatory submissions for life sciences clients
Domain
Clinical research / Life sciences
Required skills
Site monitoring, subject recruitment planning, protocol administration, quality evaluation, regulatory submission tracking, data query resolution
Preferred skills
Knowledge of clinical research regulatory requirements
Technologies
Case report forms (CRF), regulatory submission systems
Responsibilities
Performing site selection, initiation, monitoring and close-out visits; Supporting subject recruitment plan development; Administering protocol and study training; Evaluating site practice quality; Tracking regulatory submissions and data queries
Seniority
Mid-level, hands-on IC
