Clinical Research Monitor

Job Summary

A company is looking for a Clinical Research Monitor to support clinical research studies.

Key Responsibilities:

• Monitor protocol and regulatory compliance of clinical research studies across multiple treatment areas
• Review research data for accuracy and manage documentation and study milestones
• Write monitoring reports and assist in developing risk monitoring plans and study-related documents

Required Qualifications:

• Bachelor's degree in a relevant area required
• Minimum of 2+ years of clinical research experience in a complex disease area
• Prior experience managing clinical trial regulatory documents
• Preferred clinical research monitoring experience
• Preferred medical writing experience