Clinical Research

• Manage clinical research activities at investigative sites participating in Worldwide clinical studies
• Identify and assess potential research sites
• Coordinate study start-up activities, including regulatory documentation and contract and budget processes
• Conduct PSSVs, SIVs, IMVs, and COVs
• Train site personnel on protocol requirements, data collection, and safety reporting
• Monitor site performance and support study maintenance activities
• Ensure informed consent, safety reporting, and regulatory compliance
• Partner with sites and study teams to drive data quality, participant safety, and study success
• Support site closeout activities and completion of study requirements

Explore Senior Clinical Research Associate – Psychiatry at Worldwide Clinical Trials. Review requirements and application details.