Regulatory Site Readiness Specialist I

hace 3 semanas


Buenos Aires, Argentina Fortrea A tiempo completo

A clinical research organization in Buenos Aires is seeking an individual to manage regulatory submissions and document management for clinical trials. The ideal candidate will have a degree in life sciences or equivalent experience, along with knowledge of ICH regulations and a basic understanding of clinical trial processes. Responsibilities include serving as the primary contact for investigative sites and ensuring compliance with submission requirements.#J-18808-Ljbffr



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