R (Proficient)+SDTM (Proficient)+ADAM(Expert)+Efficacy(Proficient)+TLF(Expert)+Submissions(Proficient) Develop and validate SDTM and ADaM datasets as per CDISC standards Perform statistical programming using SAS and R Generate Tables, Listings, and Figures (TLFs) for clinical studies Conduct efficacy analysis to support study outcomes Ensure accuracy, quality, and consistency of datasets and outputs Support regulatory submissions (e.g., FDA/EMA)