Site Management Associate

Job Summary

To support clinical research initiatives, the remote Site Management Associate II will manage site feasibility assessments, conduct remote monitoring visits, and oversee essential document management while ensuring compliance with regulatory requirements.

Key responsibilities

• Perform investigative site feasibility and manage site relationships to ensure compliance with ICH/GCP and regulatory requirements
• Conduct remote monitoring visits and provide site training on protocol and regulatory compliance
• Maintain the Trial Master File (TMF) and ensure timely collection and quality review of essential documents

Required qualifications

• Bachelor's degree or relevant work experience in clinical research or a health-related industry preferred
• 3+ years of relevant clinical research experience required
• Strong proficiency in Microsoft Office (Outlook, Word, Excel) required
• Aptitude for learning new computer systems required
• Basic knowledge of medical terminology desired