Clinical Study Manager

The Clinical Study Manager plays a key role in the planning and execution of SpyGlass Pharma’s clinical trials. Working closely with the Director of Clinical Research and cross-functional teams, the CSM is responsible for managing day-to-day study operations to ensure clinical studies are conducted efficiently, compliantly, and on schedule.

Requirements

• Approximately 8–10 years of clinical research or clinical study management experience within the pharmaceutical, biotech, or medical device industry.
• Bachelor’s degree in a life sciences or related field preferred.
• Experience supporting or managing clinical trials, including protocol execution, site oversight, vendor coordination, and study documentation.
• Strong understanding of clinical trial regulations, including ICH-GCP and applicable FDA and international regulatory guidelines.
• Ability to work effectively in a cross-functional, matrixed environment while managing multiple study priorities.
• Strong organizational, communication, and problem-solving skills with attention to detail.

Benefits

• Comprehensive health, dental, and vision insurance plans
• Generous paid time off
• Annual Bonus opportunity
• Stock options