About Me
I am a Senior Statistical Programmer with 3.5+ years of experience in clinical research, specializing in CDISC SDTM, ADaM, TLFs, Define.XML, and regulatory submission standards. I have worked on BABE and clinical trials Phase I III across therapeutic areas, including oncology and ophthalmology.
I help CROs, pharmaceutical companies, and biotech firms with:
✔ SDTM & ADaM Programming CDISC compliant datasets
✔ Tables, Listings, and Figures TLFs Programming
✔ Define.XML, SDRG, ADRG & Pinnacle 21 Validation
✔ SAS Macros & Automation for Efficient Data Processing
✔ Regulatory Submissions FDA, EMA, PMDA
With a strong background in SAS, SQL, and CDISC compliance, I ensure high quality, submission ready deliverables that meet industry standards. Whether you need end to end dataset development or validation support, I am here to help.
Let’s discuss how I can assist your project!
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