The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice
Job Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice.
Candidates will work with sites to drive subject recruitment plans and ensure the quality and integrity of study site practices.
The position requires managing study progress by tracking regulatory submissions, enrollment, and data query resolution while maintaining compliant documentation.
Matching Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice.
Skills & Requirements
Must-have
Good Clinical Practice (GCP) knowledge
Site monitoring visit execution
Subject recruitment plan management
Trial Master File maintenance
Regulatory submission tracking
Nice-to-have
Strong problem-solving skills
Effective time management abilities
Financial management of sites
Collaborative team communication
Adaptability to project needs
Key Requirements
Bachelor's Degree in scientific discipline or health care
At least 2 years of on-site monitoring experience
Proficiency in Microsoft Word, Excel, and PowerPoint