Local

Project

Coordinator

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

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