Study Start Up Associate II
About this role
About the Role ICON is a world-leading healthcare intelligence and clinical research organization. We’re seeking a Study Start Up Associate II to lead the initiation of clinical trials, ensuring regulatory compliance and supporting study start-up activities across sites. What You'll Do
- Lead the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.
- Coordinate and liaise with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
- Manage and maintain comprehensive and accurate records of regulatory submissions, approvals, and correspondence.
- Provide guidance and support to study teams on regulatory requirements and best practices for study start-up activities.
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