Job Summary

• Responsible for operational oversight of the site, site health and monitoring activities, and identifying and proactively mitigating site-level risks.
• Build and maintain strong, trusted relationships with investigators and site staff, serving as the sponsor primary point of contact for assigned studies.
• Collect feedback from sites and advocate for process simplification and burden reduction internally, representing the 'voice of the site' in cross-functional discussions.

Matching Summary

Salary

Base: $155,000 - $183,000; Bonus/Equity: Incentive compensation and equity may be included; Benefits: Not specified

Skills & Requirements

Key Requirements

• Bachelor's degree or equivalent in life sciences or related area
• 12+ years relevant clinical research experience
• Experience leading and managing a team
• Robust budget forecasting and management experience
• Demonstrated project management skills

Work Rights