Our client is a Integral CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Start up Specialist office based in Spain. Job Overview
Responsible for CA & Ethics Committee (EC) submission Keep up to date knowledge of GCP and ICH Guidelines for clinical research. Translation and co-ordination of translations for documents required for submissions. Supervising study conduct according to GCP requirements and all applicable laws. Key Requirements
Bachelor degree in life-science Min 1 year in EC & CA submissions within a CRO, Pharma, Biotech in Spain Experience in clinical studies phase II-III Fluent English & Spanish Excellent communication skills FTE: 1.0 Tagged as: start up jobs
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📌 Start up Specialist Spain (Madrid)
🏢 Resourcing Life Science
📍 Madrid
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