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). * You are actively leading technically Medical Writers, potentially participate in recruiting and onboarding junior writers, providing guidance and reviewing documents prepared by internal teams or external vendors to ensure quality and regulatory compliance. * You hold a degree in life sciences (or equivalent); an advanced degree (e.g., PhD or Master's) is preferred, and you bring proven experience in medical writing within clinical development with a strong focus on regulatory writing. * 30 days of vacation, discounted ticket to Germany, (e)-bike leasing, capital-forming benefits, company pension plan, disabili
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