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Senior Database Analyst - LSH


Source:
TIMESJOBS.COM
Location:
Secunderabad, Telangana
Date:
09-11-2016
Job Code:
58233067
Categories:
  • Biotechnology & Science
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Job Details

Manage the Load, Transfer and Conformance of Clinical Trial data to the NCDS Standards. For assigned Clinical trials initiate data load from OC/RDC source into the Data Warehouse and communicate with all affected parties including Quality Manager, Data Manager, Database Programmer, CRO personnel and Third Party vendors.Should be able to perform cross functional tasks ranging from Database builds, Database programming, GLIB tasks and LSH tasks activities on need by need basis and with availability of time bandwidth. Participate in Data Conformance and Data availability meetings and provide the necessary inputs on the daily operational activities.Need to have basic understanding of Metadata management and impact of data elements within Metadata and the potential impact on the study activities. Participate and contribute to the Subject Matter Experts (SME) activities, and help subject matter experts on any functionality testing activates.Help onboard, support knowledge transfer (training) and contribute to updates of Working Procedures and Guidance Documents. Work and collaborate closely with External Data Loaders and ensure that the third party data for their studies gets loaded successfully.Work and collaborate with Support LSPs on the delegated LSH activities. Novartis is an Equal Opportunity Employer.Minimum requirementsResponsible for Study Setup Activities within LSH Environment. This includes inititating all the LSH Preconformance, Conformance and Post conformance of Clinical data into NCDS Standard activities.Responsible for the Maintainence and daily operational support the LSH Data Warehouse system. For studies in scope monitor data loading and processing during study conduct, i.e. review job logs, address error / failure notifications, blinding process of Third Party data and eLoader Process; monitor staging, preconformance and conformance of all data. For database lock of studies in scope, unblind and lock staging and conforming work areas.Contribute to ongoing knowledge exchange and further development of the data warehouse, i.e. save newly created / changed LSH programs and templates for re-use and work with Study Team and data warehouse Operations Team to identify and share best practices. Manage the Load, Transfer and Conformance of Clinical Trial data to the NCDS Standards. For assigned Clinical trials initiate data load from OC/RDC source into the Data Warehouse and communicate with all affected parties including Quality Manager, Data Manager, Database Programmer, CRO personnel and Third Party vendors.Should be able to perform cross functional tasks ranging from Database builds, Database programming, GLIB tasks and LSH tasks activities on need by need basis and with availability of time bandwidth. Participate in Data Conformance and Data availability meetings and provide the necessary inputs on the daily operational activities.Need to have basic understanding of Metadata management and impact of data elements within Metadata and the potential impact on the study activities. Participate and contribute to the Subject Matter Experts (SME) activities, and help subject matter experts on any funtionality testing activites.Help onboard, support knowledge transfer (training) and contribute to updates of Working Procedures and Guidance Documents. Work and colloborate closely with External Data Loaders and ensure that the third party data for their studies gets loaded sucessfully.Work and colloborate with Support LSPs on the delegated LSH activities.
Degree: MCA/ PGDCA

Additional Degree: BE/ B.Tech (Engineering)

Experience: 3-8

Requirements

Application Programming | Business/Systems Analysis | Data Warehousing | Database Administration (DBA)
Applying for this job will take you to an external site

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