As a Medical Writer you are part of our Miltenyi biomedicine business and within the Clinical Development team. Join our highly professional team in bringing new medicines to the market. 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, NDAs/MAAs, and briefing documents). * Collaborating closely within cross-functional teams (clinical, regulatory, biostatistics, safety), you
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