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, ensuring high-quality data delivery and regulatory compliance. The role collaborates closely with cross-functional teams to support trial execution and maintain inspection readiness.

Requirements

• Drafting and managing informed consent process
• Managing site selection, patient recruitment strategies, and monitoring visit reports
• Driving risk-based mitigation plans to proactively address study challenges
• Collaborating with cross-functional teams to support trial execution and maintain inspection readiness

Benefits

• 401k Matching
• Health and welfare benefits
• Incentive plans, bonuses, and/or other forms of compensation
• Paid time off