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The Senior Clinical Research Associate monitors clinical studies, ensuring they comply with protocols and regulations while documenting progress both on-site and remotely.

The Senior Clinical Research Associate will monitor clinical studies compliance and conduct, ensuring adherence to protocols and regulations. Responsibilities include overseeing trials at sites and preparing reports.

The Senior Clinical Research Associate will monitor clinical studies, ensuring compliance with protocols, SOPs, ICH-GCP, and regulatory requirements. They will also support the development of drugs and devices that improve quality of life.

The Start Up Project Manager oversees global study start up activities, ensuring site activations and project timelines meet targets across clinical trials.

As a Clinical Operations Study Lead at ICON, you'll manage projects, lead teams, develop project plans, and mentor staff to ensure successful project execution in clinical settings.

Oversee and monitor clinical trial sites to ensure GCP and protocol compliance, conduct site visits, resolve issues, ensure data integrity, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to support trial execution.

The Senior Issue Lead manages Major Quality Event investigations, coordinates audits, ensures compliance with GCP standards, and trains Issue Leads. This role involves root cause analysis, process improvement, and leading quality assessments.

The Third Party Quality Lead manages third-party quality risks in clinical operations, ensures GCP compliance, and oversees vendor performance and quality systems.

The Quality ICM Issue Lead oversees quality event case management, leading investigations, notifications, root cause analysis, and process improvements within clinical development.

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