A global biopharmaceutical services company is seeking a Senior Medical Writer to contribute to the clinical regulatory writing portfolio. This role involves leading cross-functional teams, developing critical regulatory documents, and applying stringent compliance measures. A minimum of 5 years in regulatory writing, especially in oncology or infectious disease, is required. Ideal candidates are detail-oriented, possess excellent MS Word skills, and are capable of independently managing the authoring process while ensuring high-quality outputs.
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