Become a Clinical Research Monitoring Specialist with IQVIA, focusing on site performance and data integrity across studies. Your expertise will be essential in maintaining regulatory compliance. In this role, you'll conduct comprehensive site monitoring visits to support the execution and integrity of clinical studies.

You will assist in designing recruitment strategies, evaluate site practices, and facilitate training to ensure adherence to protocols. Your insights will help enhance quality and escalate issues when necessary. Key Responsibilities:
Perform regular monitoring visits as per regulatory standards
Assist in recruitment planning and management
Provide essential training on study protocols
Monitor site adherence to GCP and ICH guidelines
Maintain detailed documentation and follow-up reports

Requirements:
Bachelor’s Degree in a scientific discipline
CRA training or prior practical experience required
Understanding of regulatory requirements such as GCP
Adept in Microsoft Office tools
Robust organizational and interpersonal skills

Leverage your clinical research experience to advance the quality and success of trials at IQVIA.

📌 Clinical Research Monitoring Specialist Montreal (Canada)
🏢 IQVIA
📍 Canada