Site Administrator - job 1 of 3

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 collect and record patient data accurately
• 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 medical office or hospital setting
• Current certifications in GCP, IATA, and CPR may be obtained during orientation; phlebotomy certification preferred
• Proficiency in MS Office and medical terminology
• Valid category B driver's license