Clinical Research DirectorAs a Clinical Research Director, you will be responsible for overseeing the planning, execution, and completion of clinical studies in accordance with regulatory guidelines. This involves coordination and management of multicenter applications with authorities and ethics committees, including document preparation and administration for pre- and post-market studies.You will also contribute to scientific publications and publication strategy, including storyline development, and prepare and manage safety reports as part of your key tasks.Key Responsibilities:Lead project teams for process optimization, documentation improvement, and data preparationManage multicenter applications with authorities and ethics committeesCoordinate document preparation and administration for pre- and post-market studiesContribute to scientific publications and publication strategyPrepare and manage safety reportsRequirements:Masters' degree or higher in Life SciencesAt least 2 years of professional experience as a Clinical Research Manager, ideally in the field of medical devicesGood knowledge of regulatory requirements in medical technologyExperience with MS Office, review tools, reference management, and document management is an advantageVery good command of English, both written and spoken; basic knowledge of German is requiredWhat We Offer:Central locationEmployee discountsFlexible hoursInternational environmentOnboardingWorkplace well-being