Ergomed Group is a specialist clinical research organization focused on rare disease and select oncology indications, with integral presence and a collaborative culture. The Specialist, Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness and regulatory compliance. Role requires a graduate degree in Chemistry/Life Sciences or Nursing, plus at least 2 years in pharma/CRO or regulatory bodies, and strong knowledge of ICH‐GCP and
📌 Impactful study start-up & regulatory lead (Cantabria)
🏢 Ergomed
📍 Cantabria
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