Clinical Research Coordinator, KKRC (2-Year Contract)

Provide research support service for clinical trials/research in accordance to ICH-GCP and protocol requirements Independently responsible for administration of clinical trials as assigned by Principal Investigator (PI) at his/her professional discretion Assist the sponsor or PI in the submission process for CIRB &/or HSA Handle complex commercial or IITs including overseeing recruitment of subjects Ensure full accountability of study equipment and investigational products during monitoring and study close-out Assist in quality control and prepare for quality assurance Provide instructions to Finance to issue invoices and handle communications between PI and sponsor companies Attend investigator meeting and start-up meeting for trials Requirements: Degree in Life Sciences/Pharmaceutical Science and other related disciplines Fluent in written and spoken English and a 2nd language/dialect Intermediate computer skills (MS Office, Word and Excel) People-management skill, strong team-player...