CenExel Benefits Overview

Coordinate clinical trials from initiation to completion following ICH/GCP and protocol. Recruit and educate participants, schedule and collect data, perform safety assessments (vitals, EKGs, blood draws), document adverse events and deviations, manage regulatory and administrative tasks, report data to sponsors, and support protocol development and site logistics.

Oversee daily operations and administrative functions of clinical research sites, ensuring compliance, managing staff, and developing budgets to meet organizational goals.

The Quality Assurance Coordinator ensures data quality and participant safety in clinical trials, adhering to various guidelines and performing audits.