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Clinical Manager Oncological Projects (w/m/d) (DE)
review of literature and publication including written feedback reports provides expert up to date knowledge of oncology international regulations guidelines and requirements for global drug development medical information and marketing provides medical writing services for Clinical Study Protocols and Clinical Study Reports, responsible to review and to finalize clinical study documents (study protocol, CRF, Patient Information, and Informed Consent) organize submissions to Regulatory Authorities and Ethical Committees experience in managing Investigator-Sponsored Studies insights on Clinical Trial Governance boards GXP experience knowledge of international regulations good communication skills especially cross-culturally