Highly Technical, Project Management, Team-oriented, Team handling, Client facing, professional Solution Architect with 16 years of customer relationship management, project development, maintenance & support experience in Life Sciences and Healthcare (LSH) domain for client Merck & Co., Inc, Retail Banking domain for Citi bank, and ERP implementation at client site. Extensive technical experience in AWS cloud, Oracle, Oracle Exadata, PL/SQL, Linux, DevOps, CICD Pipeline, Snowflakes, MongoDB, Dynatrace, HP ALM, Remedy, ServiceNow, Jira, Git, Bitbucket, Jenkins, Terraform and Power BI tools for software development and production support level 3.
Highly skilled in managing database performance and upgrades for ongoing efficiency and achievement of corporate objectives. Innovative Solution Architect with in-depth understanding of software deployment and system design illustrated over 16 years of experience in similar roles with following Agile methodology and Waterfall Model. Excellent communication skills and extensive experience working with clients and partners. Detail-oriented team player with strong organizational skills. Ability to handle multiple projects simultaneously with a high degree of accuracy. To seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills.
AWS Certified Cloud Practitioner (CLF-C01)
MongoDB (M100)
PSM I (Professional Scrum Master)
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Clinical Data Repository (CDR) : The Clinical data repository project is a key component of the Merck collaborative clinical development technology platform initiative within Clinical and Regulatory Information Services (CRIS). The high-level goals of the strategy are to improve productivity and reduce cycle time for all stages of clinical trials through improved processes and a move towards industry standards. The Clinical data repository is constructed in a coupled manner to both publishing and subscribing applications to support ‘plug-and-play' access to tools and services with the help of TIBCO system. Full and Incremental patient data flow is designed in five stages (schema) with following ETL & ELT data warehouse concept to published data into SDTM formate for FDA submission.
Controlled Terminologies Impact Analysis Tool (CTIAT): The CTIAT is focused around reducing the time it takes to implement new terms published by CDISC. CTIAT is used to generate Reports to compare a new CDISC Controlled Terminology version with existing data, which are obtained from different SharePoint sites, to determine what forms/terms need to be updated.
Analysis and Reporting Submissions Translation (ARST): The ARST system is intended to support Study Level Define file translation from English to Local Language Term through Data Translation Management (DTM) Module. The application is only support Chinese Simplified translations.
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Tool & Technology used :Form Developer 10 G , Oracle 10G, PL/SQL.
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