Clinical Research Site Administrator

Job Summary

A company is looking for a Site Administrator to support the daily operations of clinical trials.

Key Responsibilities

• Assist with the coordination and execution of clinical research studies in compliance with protocols and regulations
• Collect and record patient data accurately and maintain up-to-date study documentation
• Monitor study participants and ensure all activities follow Good Clinical Practice (GCP) guidelines

Required Qualifications, Training, and Education

• High school degree or equivalent
• Experience in a medical office or hospital setting for at least 1 year
• Current Good Clinical Practice (GCP) certification may be obtained during orientation
• Phlebotomy certification is preferred
• Valid category B driver's license