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The Administrative Assistant supports clinic operations by managing administrative tasks, coordinating meetings, processing expenses, and handling data reporting.

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

The Operations Quality Specialist provides support to Clinical Research Associates, ensuring protocol compliance, managing investigational sites, and tracking study data and documentation while assisting with site training and audits.

The Contract Analyst I will manage client contracts and change orders, coordinate with various teams, and support project financial analysis.

The Clinical Research Associate is responsible for site management, ensuring protocol compliance, monitoring patient safety, and facilitating communication between the sponsor and investigational sites.

The Clinical Supply Operations Specialist manages clinical supply logistics, including inventory tracking and documentation, vendor interactions, temperature excursions, and expiry management across trials.

Lead monitoring of clinical trials, ensuring adherence to protocols and standards. Conduct site visits, collaborate with teams, and train site staff. Build relationships for effective trial operations.

The Director of Business Development will drive sales in ICON's Patient Centered Sciences group, managing client relationships, sales processes, and revenue growth.

The Senior Clinical Trial Manager oversees end-to-end trial delivery, manages stakeholders, ensures site alignment, and collaborates for operational excellence.

As a Senior Clinical Trial Manager, you will manage clinical trial operations, oversee budgets, develop monitoring plans, drive enrollment, and foster relationships with stakeholders.