CenExel Benefits Overview

Coordinate and support clinical trials from initiation through completion, ensuring compliance with ICH/GCP and protocol. Schedule and document subject visits, collect and report data, perform safety/efficacy assessments (vitals, EKGs, blood draws), manage regulatory and administrative tasks, educate participants, and communicate with sponsors and vendors.

Supports Clinical Research Coordinators by preparing participant visits, maintaining patient charts and study inventories, completing data entry and query resolution, assisting with assessments (e.g., blood pressure, urine collection), communicating with participants and vendors, and performing clerical and monitoring-visit support while following ICH/GCP, protocol, and site procedures.

Collects and processes clinical trial specimens per protocol, maintains chain-of-custody and inventory logs, monitors sample storage temperatures, prepares collection supplies, assists lab manager with site readiness, packs and ships study materials, and documents all laboratory procedures and sample handling.