Intern
GURUS LLC
07.2024 - 09.2024
- I have acquired extensive knowledge in clinical trials and the pharmaceutical cycle, with a strong emphasis on data integrity and clinical standards.
- Standardized clinical raw data in accordance with the Study Data Tabulation Model (SDTM) standards, ensuring compliance with industry guidelines.
- I generated tables, listings, and figures (TLF) using R programming to provide clear and accurate insights from clinical data.
- I performed Case Report Form (CRF) annotation using Adobe Acrobat to ensure that the documentation aligns with clinical protocols.
- Converted Study Data Tabulation Model (SDTM) datasets to Analysis Data Model (ADaM), facilitating a seamless transition from raw data to analysis-ready datasets.
