Grifols, S.A invites a Clinical Drug Safety Officer for a temporary position. The role focuses on safety data collection, adverse event review, and acting as the pharmacovigilance representative for clinical studies. Strong communication and collaboration with clinical teams are essential.
You will contribute to safety management plans, DSUR/PSUR/RMP preparation, and support audits. Fluency in Spanish and English, plus a health sciences degree and CRO/pharma experience, are required.
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📌 Pharmacovigilance Specialist — Hybrid (Barcelona)
🏢 Grifols
📍 Barcelona
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