Jobs at ICON plc

As a Clinical Research Associate, you'll conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with investigators.

The Clinical Site Associate supports site management for clinical trials, ensuring compliance and quality in study activities, documentation, and communication with stakeholders.

As a Senior Clinical Research Associate, you'll oversee clinical trial activities, ensuring compliance with protocol and regulatory standards while managing site performance and supporting trial execution.

As a CRA II, you will design and analyze clinical trials, conduct site visits, ensure protocol compliance, and collaborate with investigators while maintaining data integrity and patient safety.

As a CRA II, you'll conduct and monitor clinical trials, ensure compliance and data integrity, and collaborate with site staff and investigators.

The Senior Contract Analyst manages contract agreements, ensures compliance, collaborates with stakeholders, analyzes contract terms, and maintains contract records.

The Site Activation Lead manages site start-up and activation activities, oversees feasibility, contract negotiations, and ensures compliance with regulations during clinical trials.

The Senior Clinical Contracts & Budget Associate manages contracts and budgets for clinical trials, negotiates terms, and ensures compliance with regulations.

The Study Start-Up Specialist will manage study initiation, drive regulatory compliance, support project teams, and ensure patient safety in clinical trials in Australia.

The In-House Clinical Research Associate provides centralized support to CRAs, manages site activities, performs remote monitoring, and assists with study start-up activities, ensuring compliance and quality in clinical trials.

The Clinical Trial Contract Associate manages site contract activities, drafting and negotiating agreements, collaborating with teams, and ensuring compliance with regulations.