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Ergomed
Ergomed is seeking a Senior Specialist, Study Start Up and Regulatory Affairs to lead and coordinate all activities ensuring site initiation readiness. You will provide expertise, ensure regulatory compliance, and act as a key liaison between internal teams, clients, and external stakeholders. Responsibilities include managing regulatory milestones, preparing essential documents, and coordinating across countries to deliver timely, compliant SSU activities in complex trials. #J-18808-Ljbffr
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