Job Summary

• Engage in a structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits.
• Under close supervision, perform site monitoring visits including selection, initiation, monitoring, and close-out.
• Manage study progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.

Matching Summary

Skills & Requirements

Key Requirements

• Bachelor's Degree in scientific discipline or health care preferred
• Equivalent education, training and experience accepted
• Prior clinical experience preferred
• Proficiency in Microsoft Word, Excel and PowerPoint
• Written and verbal communication skills
• Organizational and problem-solving skills
• Advanced knowledge of GCP and ICH guidelines

Work Rights