Goal: To equip clinical research professionals with the knowledge and practical skills needed to effectively conduct and support clinical trial monitoring activities in accordance with Good Clinical Practice (GCP) and regulatory requirements, ensuring participant safety, data integrity, protocol compliance, and inspection readiness. 

Member Rate: $645.00

Non-Member Rate: $695.00

Objective: To provide participants with a comprehensive understanding of clinical trial monitoring, including regulatory requirements, Good Clinical Practice (GCP) principles, risk-based monitoring strategies, and best practices for identifying and managing compliance issues to support high-quality, inspection-ready clinical research. Please contact us with any questions or concerns at [email protected].

Learning Objectives: Upon completion of the workshop, the attendee should be able to:

• Understand the purpose of clinical trial monitoring and the regulatory requirements
• Apply Good Clinical Practice principles during monitoring activities and monitor prep
• Evaluate participant safety and data integrity through monitoring practices
• Describe risk-based monitoring approaches
• Identify, document, and manage non-compliance findings
• Utilize monitoring as a key component of inspection readiness and overall quality management

Please book your Hotel Room here: 2026 SOCRA Project Management & Monitoring/GCP Conferences - Start your reservation

Please contact us with any questions or concerns at [email protected].