Join ICON plc as a Senior Clinical Research Associate, dedicated to high standards in clinical trials. Leverage your expertise in monitoring to drive innovation in healthcare research.
In this senior role, you will lead the monitoring of clinical trial sites to ensure compliance with regulatory requirements and GCP standards. You will be at the forefront of conducting site visits, assessing site performance, and collaborating with cross-functional teams. Your insights will enhance data integrity, while your training initiatives will uplift trial execution standards.
Key Responsibilities:
• Monitor compliance with clinical trial protocols
• Conduct site performance assessments and resolve issues
• Collaborate on data collection and reporting efforts
• Provide training for clinical staff on trial conduct
• Foster strong relationships with site personnel
Requirements:
• Bachelor’s degree in a relevant scientific field
• Proven experience as a Clinical Researc...