Senior Medical Writer, Global Regulatory

7 giorni fa

Venezia, Italia Worldwide Clinical Trials A tempo pieno

A leading clinical research organization in Italy is seeking a Senior Principal Medical Writer to prepare and lead the development of Phase I-IV study documents.The ideal candidate has a degree in life sciences, at least 4 years of medical writing experience, and excellent English skills.This role involves project management, regulatory compliance, and collaboration across departments.Opportunities for training and career development are provided.#J-*****-Ljbffr

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