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 general CRO environment.
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📌 Global Auto Regulatory Affairs Manager (Remote + Flexible Hours) - Remote (Alcobendas)
🏢 Tüv Rheinland Group
📍 Alcobendas
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