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Clinical Operations Specialist

ICON plc • Blue Bell, PA, US • published 2026-10-11 15:03:12.582629

Description

Clinical Operations Specialist At ICON Strategic Solutions, you will work in a sponsor\-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies. **What You Will Do:** You will contribute to site start\-up and activation activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: * Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications. * Coordinating and liaising with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation. * Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals,...

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