Axxonis Pharma AG Information

1) Project management of phase II and III clinical trials: * Coordination of CROs, control of budget and timelines, documentation * Development of study materials (study protocols, patient information leaflets etc.) * Organization of investigator meetings * Establishing and maintaining relations with clinical investigators and opinion leaders * Implementation of measures to accelerate patient recruitment in clinical trials * Medical assessment and quality control of clinical safety data, control of adverse event reporting requirements * Participation in company’s due diligence meetings * Development of product package designs, patient information leaflets and trade names for Marketing Authorization Applications to EMEA 2) Establishing the press office: * Creation and update of several internet presences, * creating the companies appearance (e.g. co-creating the company’s logo), * Creation of concepts for patient recruitment and new way of investigator recruitment for studies. * Contributions to scientific publications and company presentations * Development of promotional materials and activities for scientific congresses