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
• Screen and recruit study participants and assist with data entry of clinical trial information
• Maintain accurate study documentation and ensure all activities follow Good Clinical Practice (GCP) guidelines

Required Qualifications

• High school degree or equivalent
• At least 1 year of experience in a clinical research setting
• Proficiency in clinical research and general medical terminology
• Current certifications in GCP, IATA, and CPR may be obtained during orientation
• Valid category B driver's license