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As a Clinical Research Associate II, you will conduct monitoring visits for trials, ensure compliance, and collaborate with site staff to maintain data integrity and patient safety.

As a Clinical Research Associate, you will conduct site selection, manage study sites, ensure compliance, and support trial conduct, requiring 12+ months of monitoring experience.

As a Clinical Site Associate, you'll manage site communications, maintain TMF and ISF accuracy, ensure compliance, and support CRAs with site relations and audits.

The CRC Nurse conducts clinical trial procedures, collects and documents patient data, assists in recruitment, and provides nursing support while ensuring compliance with protocols and regulations.

As a Senior Clinical Research Associate at ICON, you will oversee clinical trial activities, ensuring compliance with protocols and regulations while ensuring participant safety and data integrity.

The Clinical Site Associate supports clinical trial operations, ensuring site compliance, managing documentation, coordinating trainings, and preparing for audits.

Oversee and manage clinical trial activities, ensuring compliance with protocols and regulations, while providing support and training to site staff.

The Senior Statistical Programmer analyzes clinical trial data, develops and validates SAS programs, collaborates with biostatisticians, and ensures compliance with regulatory standards.

The Financial Accountant II will manage GL finance in projects, ensure finance requirements are integrated, support closing processes, improve finance efficiency, and lead transformation initiatives.

Support the preparation and tracking of regulatory documents for site activation in clinical research. Collaborate with stakeholders to optimize study performance and ensure compliance with ICH/GCP guidelines.