- SAS Certified Professional with over 11 years of pharma and biotech industry experience in analysis, design, development, validation and testing of applications
- Extensive use of SAS Programming and Data Management in analyzing data from Phases (I 鈥� IV) clinical trials and generating TLG for interim analysis purpose and for regulatory submissions
- CDISC Standards, Annotated CRF
- Performance optimization using data cleaning and validation and complex nested macros for reporting
- Good working knowledge with Clinical study documentation like protocol, CRF, SAP, Table shell etc.
- Knowledge of writing and implementing SOPs with respect to ICH and GCP Guidelines.
- Worked closely wi...
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