Senior Clinical Research Associate

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