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The Clinical Research Associate will conduct clinical trial visits, ensure protocol compliance, analyze data, and prepare study documentation while collaborating with site staff.

Manage and lead projects ensuring successful execution. Develop project plans, mentor teams, and collaborate with stakeholders to achieve goals.

As a Clinical Research Associate, you will monitor clinical trials, ensure protocol compliance, and collaborate with investigators while analyzing medical data.

Oversee and manage clinical trial activities, ensuring adherence to protocols, regulatory requirements, data integrity, and participant safety. Conduct site visits, provide support, and maintain relationships with stakeholders.

As a Clinical Research Associate, you will conduct and monitor clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff and investigators.

As a Clinical Research Associate, you will conduct site visits for clinical trials, ensure compliance, and analyze clinical data. Collaborate with investigators, maintain data integrity, and contribute to study documentation.

As a Senior Clinical Research Associate, you will oversee clinical trials, ensuring adherence to protocols and regulatory standards, managing multiple sites, and collaborating with teams for data integrity and compliance.

The Clinical Research Associate will design and analyze clinical trials, ensure protocol compliance, and maintain data integrity during studies.

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

As a Senior Lead Data Manager at ICON, you will lead data science projects, design strategies for clinical trial analysis, and mentor team members while collaborating with stakeholders to provide actionable insights.