**Job Description**

**Primary activities include, but are not limited to:**

Assumes the responsibilities for all clinical programming (including reporting and analytics) deliverables including Oracle, Veeva platforms along with the external data captured in support of the clinical studies.

**Coordinates and participates in the following activities:**

+ Design, build, maintain, test, and document data review based on written specifications established by Global Clinical Data Management, Clinical Research and Global Safety.
+ Review the technical feasibility of study team proposed programming/reporting and technically implements them.
+ Work effectively among team to communicate issues and ideas to improve the business along with understanding of Protocol .
+ Support the development & reporting for data cleaning, medical review, clinical monitoring, and safety reports for quality and timely availability in support of our customer needs.
+ P...