SAS Base and SAS Advance Certified Consultant having experience in performing analytic SAS/statistical programming for clinical trials for client companies using SAS on Windows and UNIX platforms.
Statistical programming related to the design, programming, implementation, maintenance, and validation of Clinical trial information for the submission to the FDA during various phases. Developed study specific edit checks.
Expertise in ISS and ISE studies in creating safety analysis datasets and efficacy analysis datasets.
Developed Edit Checks and Validation to clean the database using SAS Procedures, Macros, and Reports for Clinical Data management.
Generated Ad-Hoc Reports for post Market...
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