Clinical Study Coordinator: Documentation & Compliance

Link-Worldwide in Ciudad de México is seeking a Clinical Study Administrator (CSA) to assist in the coordination and administration of clinical studies from start-up to close out. This role involves ensuring the quality and consistency of study deliverables while maintaining compliance with ICH-GCP and local regulations.
The ideal candidate should have strong organizational skills, experience in the clinical trial documentation process, and the ability to track and manage multiple tasks effectively. This is a crucial role for the successful execution of clinical trials.
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