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As a Global Study Manager at ICON, you will lead project management activities, develop plans, manage cross-functional teams, and ensure successful project execution.

The Global Study Manager will lead project management activities, develop plans, guide teams, and collaborate with stakeholders to achieve project goals in oncology clinical research.

The Global Study Manager oversees project management activities in oncology, ensuring successful project execution by leading teams, developing project plans, and maintaining stakeholder communication.

The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with site staff and investigators.

The Senior Clinical Research Associate will manage clinical trials, ensure compliance, analyze data, and collaborate with study personnel while traveling extensively.

Lead and oversee Phase I-II clinical trials as the Senior Principal Biostatistician, providing statistical input and mentoring junior statisticians.

Senior Site Monitor responsible for planning and conducting on-site and remote monitoring across Phase I-IV studies. Ensures site compliance with protocol, data quality, and participant safety, conducts source data verification, manages site communications, supports RBQM processes, and participates in audits and inspections.

Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance and data integrity. Collaborate with investigators and prepare study documentation.

The Clinical Research Associate will conduct site visits, ensure protocol compliance, review data, and collaborate with investigators to facilitate clinical trials.

As a Global Study Manager, you will oversee clinical budgets, develop monitoring plans, manage study start-ups, drive enrollment, and foster relationships with stakeholders.