Description
The Clinical Trial Manager will build and maintain engagement with investigators and site staff, manage studies and processes to agreed quality and timelines, proactively identify and mitigate study and site risks, and apply knowledge of the clinical development process and study design. The role requires previous scientific or regulatory medical writing experience, strong communication and problem-solving skills, fluency in English and the host-country language, at least five years of clinical practice experience, and a bachelor's degree in a biomedical discipline or equivalent education.
