We are looking for an experienced Clinical Research Associate, willing to work within the field of oncology. The Senior Clinical Research Associate will Perform site qualification, site initiation, and closeout visits, ensuring regulatory and protocol compliance. Visits may be on-site or remote.

As a Clinical Research Associate, ensure clinical study sites comply with protocols and guidelines. Conduct site visits, facilitate subject enrolment, and address site-related issues. Ensure safety reporting, assist in audit preparation, and maintain relationships with investigators. ICON values diversity and offers competitive benefits.