Site Activation & Regulatory Submissions Coordinator

Syneos Health, Inc. is seeking a professional to oversee the start-up processes of investigative sites for clinical trials in Buenos Aires. This role involves ensuring compliance with local regulations and submission timelines, while acting as a liaison between investigational sites and functional leads. The successful candidate will handle contracts, budgets, and necessary documentation, ensuring all activities align with quality standards.

Your ability to communicate effectively and manage regulatory tasks will be crucial for ensuring timely site activation. This role offers a dynamic environment supporting clinical research efforts.