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 of site practices and manage regulatory submissions, recruitment, and data query resolution.
The position requires maintaining accurate documentation for the Trial Master File and ensuring Investigator's Site File compliance.
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 and regulatory adherence
Nice-to-have
Oncology study experience preferred
Strong problem-solving skills
Effective time management abilities
Key Requirements
Bachelor's Degree in scientific discipline or health care