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 evaluate the quality and integrity of study site practices and escalate any quality issues as appropriate.
The position requires managing study progress by tracking regulatory submissions, enrollment, and data query resolution while maintaining accurate 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
4 years on-site monitoring experience
Protocol adherence evaluation skills
Trial Master File maintenance
Subject recruitment plan management
Nice-to-have
Oncology studies experience preferred
Strong problem-solving abilities
Effective time management skills
Collaborative team working style
Key Requirements
Bachelor's Degree in scientific discipline or health care