Advance your career with ICON plc as a Senior Clinical Research Associate, overseeing clinical trial monitoring activities. This role emphasizes quality assurance and compliance across multiple sites.
In this dedicated sponsor position, you will manage and lead clinical trial monitoring ensuring compliance with regulatory requirements and GCP standards. You will be responsible for conducting site evaluations, training personnel, and streamlining data management across sites, fostering an environment of continuous improvement and excellence.
Key Responsibilities:
• Lead monitoring efforts to uphold trial standards
• Perform site visits to assess site execution and compliance
• Collaborate with cross-functional teams to ensure data integrity
• Provide support and training to CRA colleagues and site staff
• Build and maintain effective relationships for trial success
Requirements:
• Bachelor’s degree in a relevant field
• Extensive experience as a Clinical Re...