Medical Writer II, X-TA
This role involves authoring and coordinating regulatory medical writing documents across key therapeutic areas such as Oncology, Immunology, and Neuroscience. The Medical Writer II will produce clinical study reports, protocols, and investigational brochures, ensuring compliance with ICH guidelines and internal standards. They will collaborate with cross-functional teams, contribute to document planning and review, and support quality control processes while adhering to regulatory and scientific best practices.