Worldwide Clinical Trials is seeking a Specialist, Regulatory Compliance to review and approve essential documents for study initiation in line with SOPs, country regulations, and industry best practices. The role requires strong English skills, organization, and the ability to manage multiple tasks with accuracy.
The adecuado candidate has a university degree and at least 1 year of relevant experience, with proficiency in Word and Excel.
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📌 Global Regulatory Compliance Specialist (Santa Fe)
🏢 Worldwide Clinical Trials
📍 Santa Fe
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