Jobs at ICON plc

The Senior Clinical Project Manager will lead and manage clinical projects, ensure successful execution and delivery, mentor team members, and develop project documentation, while collaborating with stakeholders and staying current with industry trends.

As a Clinical Project Manager, you will lead project activities, manage timelines, budgets, and resources, while ensuring project delivery aligns with organizational goals.

The Senior Clinical System Designer will design, implement, and enhance clinical systems, ensuring alignment with protocols, mentoring colleagues, and overseeing system performance.

The Global Study Manager oversees clinical trials, ensuring compliance and quality delivery while collaborating with cross-functional teams and analyzing medical data.

As a Laboratory Assistant, you will support laboratory operations, prepare samples and reagents, maintain equipment, and assist with tests, ensuring a compliant environment.

As a Senior CRA, oversee clinical trial activities ensuring adherence to protocols, regulatory requirements, and industry standards, while managing multiple sites and guiding CRAs.

As a Clinical Research Associate, you will conduct site visits, ensure data integrity and patient safety, and collaborate on study documentation.

The Senior Clinical Systems Lead will oversee design, development, and implementation of clinical systems, managing day-to-day operations and cross-functional coordination to improve clinical trial efficiency.

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

Oversee execution of clinical trials, ensuring efficiency and compliance while leading operations, monitoring metrics, and mentoring staff.

As a Clinical Research Associate I, you will monitor clinical trials, coordinate activities, maintain documentation, and ensure compliance with regulatory standards.

The Clinical Site Associate will support site management activities, including document tracking, site communication, and coordination of site visits for clinical trials.

As a Clinical Research Associate I, you will coordinate clinical trial activities, ensuring compliance with guidelines, and maintain documentation and relationships with stakeholders. Active monitoring and prompt query resolution are key responsibilities.

Manage clinical operations for assigned studies, ensuring adherence to quality, timelines, and budget while fostering relationships with key institutions and optimizing diverse recruitment efforts.

As a Clinical Research Associate I at ICON, you will monitor clinical trials, coordinate activities, maintain documentation, ensure compliance, and build relationships with stakeholders.

The Clinical Trial Manager will oversee the planning and execution of clinical trials, ensuring compliance with regulations while managing budgets and relationships with trial investigators.

As a Principal Biostatistician, you'll design clinical trials, analyze complex data, oversee statistical activities, and contribute to innovative treatments.

The Senior Clinical Trial Manager oversees clinical trials, manages budgets, ensures study integrity, optimizes team performance, and develops relationships with stakeholders.

As a Clinical Research Associate II, you will monitor clinical trials, ensure protocol compliance, and analyze medical data while ensuring patient safety.

The Clinical Site Associate conducts remote site management activities, ensures data accuracy, assists with investigator recruitment, and maintains professional relationships with study teams and sites.