2026 CRA ADP Beijing Shanghai

Engage in a structured training program to gain knowledge and skills required to conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.

Requirements

• Complete therapeutic, protocol and clinical research training
• Gain experience in study procedures by working with experienced clinical staff
• Administer protocol and related study training to assigned sites
• Evaluate the quality and integrity of study site practices
• Manage the progress of assigned studies
• Create and maintain documentation regarding site management, monitoring visit findings and action plans
• Collaborate and liaise with study team members for project execution support