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 must work with sites to adapt and track subject recruitment plans to enhance predictability while ensuring data integrity.
The position requires managing study progress by tracking regulatory submissions, enrollment, and resolving data queries while maintaining the Investigator's Site File.
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
On-site monitoring experience
Protocol and regulatory adherence
Subject recruitment plan management
Trial Master File maintenance
Nice-to-have
Mentoring new or junior CRAs
Strong problem-solving skills
Effective time management
Collaborative team relationships
Financial management of sites
Key Requirements
Bachelor's Degree in scientific discipline or health care