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As a Clinical Research Associate II, you will conduct site visits, ensure protocol compliance, and collaborate with investigators while preparing study documentation.

As a Clinical Research Associate, conduct site visits, ensure compliance and safety, collaborate with staff, and review clinical data documentation.

The Senior Clinical Research Associate will manage clinical trials, ensure compliance, analyze data, and collaborate with study personnel while traveling extensively.

The Clinical Trial Manager II will oversee all facets of clinical trials, ensuring compliance, analyzing data, and collaborating with teams to optimize operations and outcomes.

The Senior Clinical Research Associate will oversee clinical trials, ensuring protocol compliance, data integrity, and patient safety, while collaborating with investigators and performing data reviews.

The Senior Clinical Research Associate will conduct site visits, ensure protocol compliance, collaborate with site staff, and manage clinical trial documentation.

The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with site staff and investigators.

The Contract Senior CRA will conduct various clinical trial activities, ensure compliance, and collaborate with site staff to maintain data integrity.

Responsible for the oversight of contracts and budgets in clinical studies. Duties include budget strategy, FMV governance, documentation management, and cross-functional collaboration.

As a Senior Clinical Research Associate at ICON, you'll oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements while managing multiple sites and projects.