Study Coordinator

Study Coordinator


  • 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;


  • 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