Clinical Research Associate 1 - CFSP

About this role

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits after completing training period
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
• Collaborating with experts at study sites and with client representatives