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Clinical Project Manager (m/w/d) (DE)

Clinical, Pharma, Top 100 CISA

Your Tasks Plans, conducts, supervises and evaluates clinical trials phase I - III Leads Clinical Trial Team Ensures that clinical trial is conducted according to proto­col, SOPs, ICH/GCP and other regulations Plans and supervises trial timelines and budget Ensures oversight of all trial-related activities outsourced to CROs Develops and implements all trial-related documentation and plans Supports process improvement and SOP generation from a clinical operation perspective Your qualifications Academic degree in medicine or life science Several years of international experience as Clinical Project Manager for clinical research phase I - II Experience in oncology/hematology preferred Strong clinical operation skills and process-oriented mind­set Excellent communication skills both in written and spoken English and medium communication skills in German

map Hamburg, date_range ab sofort update Permanent

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