Leading the clinical studies and medical affairs department, Coordinating and monitoring of project and study plans and associated work packages, including timelines, budget and resource allocation, Creating and maintaining a comprehensive overview of all ongoing studies and providing regular status updates to general management, Supporting the development of global clinical registration strategies, Identifying and recommending external project and cooperation partners, including KOL management, Reviewing interim study results, final study reports and interpreting study outcomes, Reviewing and monitoring the analysis, provision and documentation of scientific and medical data for regulatory approval processes and regulatory requirements (including preparation of submission dossiers for IRBs and regulatory authorities), Overseeing the creation of clinical evidence and conducting literature research for clinical evaluations, including proof of clinical marketing claims
