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Manage clinical systems implementation and maintenance, ensuring compliance with regulatory standards and improving data collection processes. Collaborate with teams and support training efforts.

Lead the design and management of clinical trial systems, ensuring data integrity and compliance while collaborating with stakeholders.

As a Senior GCP QA Manager, the role involves leading quality event investigations, managing compliance issues, and improving clinical operations while liaising with various stakeholders.

The role involves providing DMPK expertise, conducting reviews of nonclinical programs, preparing regulatory submissions, and engaging in business development initiatives.

The Senior CRA oversees clinical trial activities, ensuring protocol adherence, data integrity, and compliance, while managing site relationships and conducting site visits.

The Associate Outsourcing Manager develops and implements procurement strategies, partners with teams for needs assessment, negotiates contracts, manages supplier relationships, and monitors processes for improvements.

As a Senior Clinical Research Associate at ICON, you will manage clinical trial activities, ensuring compliance with protocols and regulations, while monitoring site performance and supporting staff.