Job Description

Key Responsibilities:

• Coordinate and oversee the execution of clinical research studies from start-up to close-out
• Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements
• Manage study documentation, including IRB submissions, source documents, and regulatory binders
• Recruit, screen, and consent study participants
• Collect, enter, and verify clinical data
• Monitor patient safety and report adverse events
• Liaise with sponsors, monitors, and regulatory bodies
• Train and mentor junior CRCs and research staff
• Participate in audits, monitoring visits, and sponsor meetings
• Maintain accurate study records and timelines

Job Tags

Similar Jobs