Job Description
 To implement Oracle Clinical products/modules. To work closely to build Database in Oracle Clinical, which adhere to standard and facilitate Data collection, Data cleaning and Statistical analysis. To work on Remote Data Capture and AERS methodologies To possess good knowledge of Front end and Back end of Oracle clinical Application with a proactive approach to get the complete study done.  To Involve in clinical studies which includes: Clinical study set up, Standard Study Design, Patient Details, Glib objects (DVG, Questions/Question Grps/Question Sets), DCMs/DCIs, Data entry screens, Validation & Derivation Procedures, External data loading, Data Extraction, views and Batch Data loading To Create and Teste Validation and Derivation procedures using OC application and using custom code with PL/SQL and SQL, in order to maintain data accuracy and track the results of the drug trail in accordance with SOP, DMP and 21CFR Part 11. To involve in creating & testing application according to the study design document & CRF To manage pharmaceutical data and evaluate Clinical Data Coordinator request to gather additional information and generating various reports relating to clinical studies. To generate various Clinical Trials reports using Integrated Review 6.0.5 for SRS (Standard Reporting System) analysis  Ad-hoc programming in a client server (windows NT-Unix) environment using PL/SQL,SAS, SAS/SQL and SQL Work closely on CTMS related modules to sort out operational issues and provide ad-hoc technical
Education : UG - Any Graduate
Contacts : Pushpa Oracle India Pvt Ltd Oracle Technology Park # 3, Banerghatta Road Bangalore,Karnataka,India 560029
Ph : 080-40298235,Email pushpalatha.sreenivasan@oracle.com
Website http://www.oracle.com
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