To enlarge our Clinical Regulatory Affairs Team we are looking as soon as possible for a * Develop clinical trial strategies, shaping study designs based on regulatory requirements, competitive insights and company's research interest. * Give insights into clinical data sets and evidence for our company's products to internal stakeholders. * Assess clinical study ideas and initiatives as well as act as for the respective internal approval process. * Keep record of clinical initiatives, grants and data collections in the field. * Define data endpoints and sample sizes (together with clinical evaluation team and support of biostatistics) for data collections, studies and clinical initiatives. * Author and review study synopses and clinical trial protocols, regulatory documents, and study-related publications for clinical initiatives and grants.
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