Description
The Clinical Trial Manager is responsible for building engagement with investigators and site staff, managing studies and processes to agreed quality and timelines, proactively identifying and mitigating study and site risks, and applying knowledge of the clinical development process and study design. The role requires at least five years of clinical practice experience, a biomedical bachelor's degree or equivalent education, scientific or regulatory medical writing experience, strong communication and problem-solving skills, fluency in English and the host-country language, and compliance with Parexel standards, ICH-GCP requirements, training, timesheets, expense reports, and CV updates.
