Noble Kumar Email & Phone Number

Overall, more than 4 years of SAS programming experience in Clinical trials. Responsibilities include the thorough understanding of SAP requirements, development of Analysis Datasets and TLF’s report generation for Phase I through Phase III clinical trials for pharmaceutical and biotechnology products in a wide spectrum of therapeutic area and has an extensive experience in CDISC (SDTM and ADaM).

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  Statistical Programmer Ii

  Sylphid Analytics Pvt Ltd

  Aug 2020 - Present - India

  Perform CDISC activities in accordance with corporate quality standards, SOPs/Work instructions/Guidelines,ICH-GCP and/or other regulatory requirements.Co-ordinate with the client for data issues, outliers, reviews schedules, etc.Ability to work on data migration from legacy datasets to standards such as CDISC and client specific requirements.Perform CRF Annotation and specification creation as per CDISC standards.Read and understand the program specifications document.Validation of SAS datasets using PINNACLE software for CDISC compliance.Prepare SAS Analysis datasets, tables, listings, and figures as per specification.Write programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc.Ensuring on-time quality delivery.Validate tables, listings, and figures as per SAP and Mock shells.Perform all the above tasks using standard operating procedures (SOPs) as defined in Quality Management system or the respective client(s) as applicable.Perform Lab and PC data Reconciliation.Works with Statisticians and researchers to implement the appropriate data analysis in SAS for a particular study

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  Jntuh College Of Engineering Hyderabad

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