Teams at ICON plc

Conduct site selection, initiation, monitoring, and close-out visits for clinical research studies. Serve as the sponsor-site contact, ensure ICH-GCP and regulatory compliance, maintain CTMS and eTMF documentation, monitor patient safety and drug accountability, support recruitment and retention, resolve data queries, track site progress and payments, and escalate risks while collaborating with clinical trial partners.

Conduct clinical trial monitoring for early-stage oncology studies, including site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; resolve data queries; and support clinical study documentation. Requires at least two years of Clinical Research Associate experience, oncology monitoring expertise, a scientific or healthcare degree, and willingness to travel up to 50% within the assigned region.

Monitors oncology clinical trial sites for protocol, regulatory, and GCP compliance; conducts site visits, resolves issues, supports trial execution, and ensures data integrity. Collaborates with cross-functional teams, trains site staff and CRAs, manages multiple sites and projects, and maintains stakeholder relationships. Requires Colorado residence, oncology monitoring experience, at least 60% domestic and international travel, and a valid driver's license.