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The Clinical Research Associate will conduct site visits, ensure protocol compliance, manage data integrity, and collaborate with site staff in clinical trials.

Lead Clinical Research Associate will oversee and manage clinical trial sites, ensuring adherence to protocols and regulations while mentoring junior staff and ensuring data integrity.

As a Clinical Research Associate at ICON, you will design and analyze clinical trials, ensure protocol compliance, and collaborate with site staff for effective study conduct.

As a Clinical Research Associate, you'll oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements, managing sites, and supporting data integrity and participant safety.

The Senior Clinical Research Associate will oversee clinical trials, ensuring compliance, maintaining data integrity, and preparing study documentation while collaborating with investigators and site staff.

The Senior Clinical Research Associate oversees clinical trial activities, ensuring compliance with protocols, regulatory requirements, and GCP standards, while managing site performance and maintaining relationships with stakeholders.

The Digital Media Buyer develops and implements digital advertising campaigns for patient recruitment, optimizing performance and collaborating on content creation.

The Clinical Research Associate will manage site interactions, conduct monitoring visits, ensure compliance, support recruitment, and oversee data management in oncology studies.