I have industrial experience in clinical trial data (Therapeutic areas: Oncology, Neurology, Cardiovascular) analysis and validation in Contract Research Organization (CRO), where I have been using the SAS programming language for the last four years.While working as a statistical programmer, I gained experience producing datasets related to the following topics:population pharmacokinetics (popPK), pharmacokinetic-pharmacodynamic (PKPD) relationships, and physiological-based pharmacokinetics (PBPK). These datasets were generated using the Study Data Tabulation Model (SDTM)/Analysis Data Model (ADaM) for NONMEM/PKsim software for phases (I–IV). Developed analysis datasets for Machine Learning purposes in Phase IV studies under the guidance of Data Scientists and Modelers. Created CDISC standard datasets ADaM and developed the ADaM specification using ADAMIG. validated the ADaM dataset by double programming along with Pinnacle 21 validation. Also, I created documentation such as the Data Specification (DS), Data Item Specification List (DISL), and NONMEM Input File (NIF) by analyzing sample documents, protocols, and Technical Guidance Documents (TGD).Along with this, Proven experience in handling projects, supervising team members and project management.Furthermore, I have one year and eight months of industry experience as an IT executive in an IT company, where I provided technical support to clients and vendors. Additionally, I have one year of work experience as an IT trainer in the web field.I accomplished a Master's degree in Information Technology (MIT) and a Bachelor of Science (Honors) degree in Computer Science and Engineering (CSE).
Listed skills include Web Development, Android Development, and Networking.