Strategic Study Start-Up & Regulatory Affairs Lead

Ergomed is a specialist clinical research organization focused on rare disease and oncology trials. The Study Start Up and Regulatory Affairs Specialist leads and coordinates all activities related to achieving site initiation readiness and regulatory compliance across assigned countries or projects.

You will act as a liaison between internal teams, clients, and external stakeholders, ensuring timely, compliant SSU delivery and high-quality regulatory documentation in a multi-country setting.

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