Senior Clinical Research Associate

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. As a Senior Clinical Research Associate, you will be responsible for conducting site monitoring responsibilities for clinical trials, providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality.

Requirements

• Guidance, oversight, and feedback to the CRA team
• Reviewing monitoring visit reports, conducting co-monitoring and evaluation visits
• Ensuring protocol compliance, addressing site questions, and assisting with study recruitment, site training, and other site-related issues

Benefits

• Flexible working hours
• Opportunity to work with a global team
• Professional development opportunities