We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. As a Medical Writer you are part of our Miltenyi biomedicine business and within the Clinical Development team. You will be responsible for the development and oversight of clinical and regulatory documents that support global drug development programs, including preparation, development, review, revision and finalization of clinical documents for submission to regulatory authorities. * You lead the development, authoring, and submission of regulatory documents (e.g., CTD modules, clinical study reports, investigator brochures, INDs/IMPDs, ...
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