Study Coordinator

Explore remote-first, flexible opportunities to join our mission to reimagine clinical trials.
Prepare study documents for Ethics committee review and approval; Schedule the on-site visits with the Sponsor; Performing study socialization and planning subject recruitment strategy; Coordinating subjects recruitment and screening; Schedule subject visit and coordinating study activities with field team, laboratory, nutritionist, and all related study personnel; Oversee the storage and accountability of Investigational Product; Maintain accurate and complete records; Close the study and archive the study records; Requirements Physician or other related medical background; Fluent in English are preferred; Have a good understanding and knowledge of Good Clinical Practice (GCP) and experiences in clinical trials are preferred; Able to organize a team or a group of trials participants; Have a good communication skill and interpersonal skill; Able to solve problems; Responsive, creative, and adaptable to manage changes; Fresh graduate are welcome to apply; Please send your CV and Application Letter by email with subject: " Study Coordinator " (space) " Applicant Name "
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