[Your tasks and responsibilities] 1. Responsible for Clinical Site Set-Up including CRO communication on IRB (Institutional Review Board) Approval, Study Contract, Site specific Informed Consent and Payment prior to planned First Patient First Visit in timely manner 2. Responsible for IRB Management during/after study period on Amendment / Annual+Others+Deviation reporting / Termination & Clinical Study Report of study 3. Responsible for Study Contract and Payment management during study period on Amendment / Termination of study 4. Responsible for monthly tracking of Study and Team payment to ensure planned budget management 5. Lead and manage Vendor Information and Study Payment related-system SRM, Your-Docs, WPA, MDG, SAP 6. Responsible for Study Contract Form and Contract List to be up-to-date which are working with Law, Patents & Compliance Team 7. Archiving Management on IRB, Contract and Payment 8. Responsible for Team Administrative and Logistic Supports [Qualifications / Requirement] - Bachelor’s degree (or equivalent) - Pharmacist or nurse or major in scientific field is preferred or at least 3 years of experience related to clinical study - Good communication, negotiation and presentation skill - Good English skill in reading/writing/listening preferred - Computer literacy: e.g. Microsoft Word, Excel, PowerPoint, Outlook. | 
