Jobs at ICON plc

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

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

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

The Senior Clinical Research Associate monitors trial sites to ensure protocol adherence, conducts site visits, collaborates with teams for data collection, and provides training to site staff.

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

Act as strategic liaison to investigator sites, build long-term relationships, support multiple studies, escalate operational issues, align site capabilities with study opportunities, monitor performance metrics, and drive site engagement and improvement initiatives.

As a CRA II/Senior CRA, you'll monitor clinical trial sites, ensure compliance with protocols, conduct site visits, support data collection, and train site staff.

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