Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
ICON plc
Overview
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
Quick view →
Compensation
Salary not listed
Posted
8 days ago
Coordinate the setup and monitoring of oncology clinical trials while maintaining accurate study documentation and reports. Build collaborative relationships with investigators and site staff to ensure patient safety and regulatory compliance.
15 days ago
