Posted on: August 30, 2024
Are you known for being well-organized and structured with a good eye for details? You will be a part our highly motivated and close-knit team, fueled by a passion for science, innovation, and making a tangible difference in people's lives. Your job will be highly varied and will amongst other responsibilities include to ensure that the regulatory process for clinical trial submission is planned and executed including management of the Clinical Trial Application documentation for international Phase I-III clinical trials.