28 sep
|
Ergomed
|
Madrid
Ergomed is seeking a Study Start Up and Regulatory Affairs Specialist in Madrid to lead regulatory readiness for site initiation, ensure ICH-GCP compliance, and liaise with internal teams, clients and external stakeholders. The role requires at least 2 years in pharma/CRO, a life sciences graduate degree, and the ability to draft/review regulatory documents, translations and site agreements.
You will develop regulatory strategy, manage timelines, identify risks, and drive submissions across
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📌 Strategic Study Start-Up & Regulatory Expert (Madrid)
🏢 Ergomed
📍 Madrid