Develop clinical trial strategies, shaping study designs based on regulatory requirements, competitive insights and company's research interest. * Assess clinical study ideas and initiatives as well as act as for the respective internal approval process. * 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. * Master's degree in biostatistics, biology, chemistry, or a comparable field of study * Several years' experience in clinical and scientific research (especially in study designs and scientific research questions)
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