CSL seeks a Principal Medical Writer to lead development of high‑quality clinical and regulatory documents for innovative therapies in serious and rare diseases and influenza prevention. In this senior role, you will own strategy, writing, and editing of CSRs, protocols, IBs, and CTD modules, ensuring compliance with ICH and global regulatory standards. You will partner closely with clinical, biostatistics, regulatory, and safety experts worldwide to interpret complex data and craft clear, patient‑focused messages. As a key contributor in CSL’s collaborative, values‑driven culture, you will mentor writers, manage document portfolios and timelines, and support publications that advance patient care globally.
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