Worldwide Clinical Trials is seeking a Regulatory Affairs professional to lead submissions across EMEA, APAC and LATAM and support business development with regulatory input. Roles include preparing technical documents, mentoring junior staff, and ensuring compliance with ICH GCP and country-specific requirements. Strong leadership and cross-cultural communication are essential for success in a integral CRO environment.
📌 Remote EMEA Regulatory Affairs Manager (Comunidad de Madrid)
🏢 Worldwide Clinical Trials
📍 Comunidad de Madrid
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