Senior Clinical Research Associate

Job Summary

Working remotely on a full-time contract basis, the Senior Clinical Research Associate will manage clinical trial activities, ensure compliance with regulatory requirements, and support client interactions throughout the product development lifecycle.

Key responsibilities:

• Manage and oversee clinical trial activities to ensure adherence to protocols and regulatory standards
• Collaborate with cross-functional teams to facilitate client communication and project updates
• Monitor trial progress and provide timely reports on study milestones and outcomes

Required qualifications:

• Proven experience in clinical research and trial management
• Strong understanding of regulatory requirements in the medical device industry
• Bachelor's degree in a relevant scientific or healthcare field
• Experience with clinical trial documentation and reporting
• Ability to work independently and manage multiple projects simultaneously