Associate

• Lead the initiation of clinical trials
• Contribute to site start-up and activation activities
• Prepare and submit regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications
• Coordinate with internal and external stakeholders to obtain approvals and authorizations for study initiation
• Manage and maintain records of regulatory submissions, approvals, and correspondence
• Provide guidance and support to study teams on regulatory requirements and study start-up best practices
• Participate in process improvement initiatives to streamline study start-up processes and enhance efficiency
• Work in a sponsor-dedicated model supported by ICON’s global expertise

Explore Study Start Up Associate 2 – Supporting North America region at ICON plc. Review requirements and application details.

Study Start Up Associate 2 – Supporting North America region

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