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Selina Schmid has extensive experience in regulatory affairs and clinical trial management, currently serving as an Expert DRA Clinical Trial Manager at Idorsia Pharmaceuticals Ltd since June 2017, following a tenure as Senior DRA Clinical Trial Manager. Prior to Idorsia, Selina worked at Actelion Pharmaceuticals Ltd, where roles included Senior DRA Clinical Trial Manager and DRA Clinical Trial Manager from 2009 to 2017. In the earlier stages of the career, Selina was a Regulatory Affairs Manager at Teva Pharma AG, with responsibilities that included preparing and submitting marketing authorization applications to the Swiss Health Authority. Selina completed education at Freies Gymnasium Bern and the University of Basel.