Clinical Research Assistant

Job Summary

A company is looking for an Assistant CRA.

Key Responsibilities

• Completes study and site management activities as defined in the task matrix
• Provides logistical support for the monitoring process and assists with site management tasks
• Coordinates study/site supply management and supports essential document collection and verification

Required Qualifications

• 1 to 2 years of relevant experience or equivalent education and training
• Basic knowledge of medical/therapeutic areas and medical terminology
• Understanding of ICH GCP and applicable regulations
• Proficiency in MS Office and ability to learn relevant software
• Experience with electronic study data systems and CTMS