Clinical Research

Monitors clinical trials at investigator sites, ensuring GCP compliance, data integrity, and patient safety across study phases.

Leads site monitoring, mentors junior CRAs, and oversees risk-based monitoring across multi-country trials.

Owns end-to-end trial delivery: timelines, budgets, vendors, and cross-functional study teams.

Manages clinical data flow, query resolution, and database lock activities for trials.

Authors clinical study reports, protocols, regulatory submissions, and scientific publications.