Site Administrator - job 1 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 and assist with data entry and scheduling of participant visits
• Maintain accurate study documentation and ensure compliance with 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
• Experience with initial IRB submission and maintenance requirements
• Valid category B driver's license