Site Administrator - job 3 of 4

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
• Screen and recruit study participants, collect and record patient data, and maintain accurate study documentation
• Monitor study participants for adverse events and ensure all study 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