Clinical Trial Coord

Under guidance, prepares, reviews, and coordinates local EC submissions in alignment with the global submission strategy. Under guidance, supports the preparation of local MoH submissions as applicable, in alignment with the global submission strategy. Under guidance, may coordinate with internal functional departments to ensure various site start-up activities are aligned with submission activities and mutually agreed upon timelines.Have contact with investigators for submission related activities or act as a key contact at country level for either Ethical or Regulatory submission related activities. Responsible for preparing Regulatory Compliance Review packages, including working with the CAS, as applicable. Coordinates other activities in support to the execution of start-up tasks such as translations, EC/MoH payments, contracts signature, etc.