Clinical Monitoring Support Associate

Job Summary

Supporting clinical trial operations, the full-time Clinical Monitoring Support Associate will manage documentation, assist with regulatory submissions, and ensure compliance in a remote work environment.

Key responsibilities

• Manage and organize clinical trial documentation and records
• Assist in the preparation and submission of regulatory documents
• Ensure compliance with clinical trial protocols and regulatory requirements

Required qualifications

• Bachelor's degree in a related field or equivalent experience
• Experience in clinical research or monitoring support
• Familiarity with regulatory guidelines and clinical trial processes
• Proficiency in document management systems and software
• Strong organizational skills and attention to detail