Artiva Biotherapeutics is seeking a Sr. Manager, Medical Writing to support clinical development, regulatory submissions, and scientific communications. The role involves authoring essential documentation and collaborating with teams across Clinical Development, Regulatory Affairs, and more to ensure compliance and scientific integrity.
Ideal candidates have a strong background in biology or related fields, with substantial experience in preparing clinical documents and a keen attention to detail.
Benefits include a comprehensive package with medical, dental, and retirement options.
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