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Clinical, Clinical Study Manager, Pharma, Top 100 CISA

Study Coordination Overall support of Principle Investigators for study management, study progress monitoring and study documentation Actively collaborate with Analytical Project Manager, Operations, Quality Control, Quality Assurance and Finance to facilitate a successful study progress and project documentation Assist in generation of reports, including compiling report material, preparing report table and data management Support in data controlling (QC), peer review of experimental results and data cross check for data submission to clients Tracking status of material and reagents including the inventory and expiry date Assist in tracking and resolution of deviations Provide sample coordination and administration including sample reconciliation Updating project tracking tools, e.g. Master Schedule Client Communications/Coordination Coordination of client communications and meetings including meeting agenda and minutes and action item tracking Coordination of external partners, e.g. for sample shipments or reagent supply Data Management Data management using Watson LIMS or equivalent systems Support report generation including processing, reviewing and creating data tables Position Requirements Education in biotechnology or natural science or equivalent Experienced in GxP (GLP, GCP, GMP, GDP) regulations Industry or CRO experiences preferred Good knowledge of MS Office Excellent Planning and Organizing skill Strong communication skills Team worker Goal-oriented working method Fluent skills in English and German (most documents are in English, TC with client is also in English)