Supports data analysis and interpretation of collected data to assess the efficacy and safety of the compound/intervention, including statistical evaluation and comparison to predefined endpoints * Supports final report preparation including compiling findings into a comprehensive Clinical Trial Report that outlines the methodology, results and conclusions of a clinical trial and which will be used for regulatory submissions * Supports Global Safety with medical expertise in the review of adverse events and safety issues, as requested * Provides support in the review of scientific publications (abstracts, presentations, and manuscripts) * Supports review of concepts for -initiated studies * A minimum of 5 years of clinical development research, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) at an international (Europe, USA, Australia) level is required
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