SpyGlass Pharma, Inc.

Research Analyst

• Conduct site monitoring visits (initiation, routine, and close-out) to ensure compliance with the clinical protocol, GCP, and regulatory requirements.
• Assist in the preparation and review of essential trial documents, such as informed consent forms, case report forms, and investigator brochures.
• Collaborate with site staff to ensure proper documentation, timely data entry, and resolution of data queries.
• Assist in the identification, selection, and training of investigative sites.
• Maintain accurate and complete study files and records in accordance with GCP and company SOPs.
• Monitor study progress to ensure timelines and quality standards are met.
• Report site activities and findings to the Clinical Study Manager and escalate issues as necessary.
• Support regulatory submissions by preparing clinical trial applications and maintaining relevant documentation.
• Work collaboratively with cross-functional teams, including Regulatory Affairs, Quality Assurance, and Project Management, to achieve study objectives.

Clinical Research Associate – All Levels