Clinical Research

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits
• Uses judgment and experience to evaluate overall performance of site and site staff
• Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance
• Verifies the process of obtaining informed consent has been adequately performed and documented
• Assesses factors that might affect subject/patient’s safety and clinical data integrity
• Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents

Single Sponsor Clinical Trial Manager I

Clinical Trial Manager I