Clinical Trial Operations Associate

Job Summary

Clinical Trial Operations Associate is a full-time position focused on supporting study startup, site management, and live-study monitoring for clinical studies involving brain monitoring devices.

Key Responsibilities

• Collaborate with project teams to support study startup activities
• Act as the primary point of contact for clinical sites to ensure smooth operations
• Monitor project progress and maintain compliance with regulatory standards

Required Qualifications

• Experience in clinical project management or clinical operations roles
• Strong organizational and project management skills
• Familiarity with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• A proactive mindset with the ability to manage multiple responsibilities
• Desire to learn more about analytics, statistics, and clinical trials