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The Senior CRA manages clinical trials, ensuring adherence to protocols and regulations, overseeing site performance, training site staff, and maintaining relationships with stakeholders.

Oversee ICON's Specialty Laboratory Operations, managing all aspects of high-complexity testing, ensuring compliance, and delivering operational excellence while also overseeing P&L responsibilities.

The Clinical Research Associate manages site contact for oncology studies, ensures compliance and safety, conducts monitoring, and supports recruitment and training efforts.

Monitor clinical trial sites, ensure adherence to protocols, conduct site visits, train staff, and manage relationships for oncology trials.

As a Clinical Research Associate, you will liaise with investigational sites, ensuring compliance, monitoring studies, maintaining documentation, and supporting recruitment efforts in oncology trials.

The Senior Clinical Research Associate will monitor cardiovascular devices, ensuring compliance with FDA regulations and managing study communication, while travelling regionally up to 65%.

The Investigator Payment Specialist processes investigator payments, maintains compliance, resolves payment discrepancies, and assists in financial reporting related to clinical trials.

Oversee and monitor clinical trial sites to ensure protocol, regulatory and GCP compliance; conduct site visits; manage multiple sites; ensure data integrity and participant safety; train and support site staff; collaborate with cross-functional teams and maintain stakeholder relationships.

As Global Study Lead, you will manage clinical trial aspects, focusing on budget oversight, study monitoring, enrollment, and stakeholder relations.

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring protocol compliance, data integrity, and patient safety, while collaborating with site staff and preparing study documentation.