[담당업무]

 Serve as the primary project contact for communication

 Oversee the development of project plan and monitoring plan against project progress

 Provide systemic management with project progress reports on project activities as requested

 Evaluate study progress by using company tracking systems, status reports, site visit scheduling,

   and project budget review as appropriate to ensure project profitability

 Ensure the expected progress and performance are on target throughout

   the study both at the project team and investigator level in accordance with the scope or work and plan

 Ensure appropriate staffing of projects and interacting with senior management where appropriate to resolve conflicts

 Be responsible for the overall coordination and management of clinical research project in conjunction with the project team

 Ensure all regulatory approvals and IRB submissions keep to projected timelines and provide immediate notification to the sponsor of any delays

 Analyze and oversees cost, personnel hours and project needs to determine the most cost effective and efficient means to successfully run and complete projects,

  while meeting the Client's needs and adhering to the contract

 May participate in prospective study feasibility assessment as required

 Manage Project team staffs  Ensure the completion of all tasks assigned to Project team staffs

 Hold a regular project team meeting and/or teleconferences

 Participate in quality improvement activities to increase overall operational efficiency

 Ensure the provision of GCP compliance input

 Support the senior project management with Project Manager

 Attend all relevant training and SOP training

[지원자격]

 Good clinical knowledge with understanding of medical terminology

 Good computer literacy with working knowledge of PCs, Windows and Microsoft Office applications, etc

 Good command of spoken and written English

 Good oral and written communication and co-ordination skills with the ability to conduct meetings

 Team oriented and organized

 Understanding of GCP and MFDS regulations

 Ability to handle multiple tasks to meet deadlines in a dynamic environment

 Previous experience of clinical research from 3 months to 3 years

   (if no experience in clinical research, it is required 3 month in-house training)