Associate Clinical Project Manager, Sponsor Dedicated

This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout. Operating in a fast-paced environment with evolving priorities, the role ensures high-quality data delivery and regulatory compliance across all phases of the trial.

Requirements

• Drafting and managing informed consent process
• Managing site selection
• Patient recruitment strategies
• Monitoring visit reports
• Driving risk-based mitigation plans

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan
• Health and welfare benefits