CenExel Benefits Overview

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.

The PRN-Clinical Research RN I oversees clinical study activities, providing nursing care to participants, documenting studies, and ensuring compliance with protocols.

The Regulatory Coordinator prepares, organizes, and implements regulatory research documents, maintains regulatory compliance, and coordinates investigator training for clinical trials.