29 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.
Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia. Si su perfil encaja, presente su candidatura.
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 xcskxlj site agreements.
You will develop regulatory strategy, manage timelines, identify risks, and drive submissions across
📌 Strategic Study Start-Up & Regulatory Expert (Madrid)
🏢 Ergomed
📍 Madrid