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Nathan George
Nathan George
Senior Statistical Programmer
Nathan George is a Senior Statistical Programmer with over 9 years of experience in clinical research and statistical programming. Skilled in SDTM, ADaM, and TLF development, he specializes in programming, validation, and data mapping to support clinical trial analysis and regulatory submissions. Nathan has worked with leading organizations including Novartis, Bayer, QuintilesIMS, and St. John’s Research Institute, delivering high-quality statistical outputs aligned with FDA, DCGI, and EC standards. Proficient in Argus Safety, WHO Drug Dictionary, and MedDRA coding, he combines technical expertise with strong analytical and mentoring skills to ensure data integrity and compliance across global studies.
FORMERLY AT
Novartis
LOCATION
Hyderabad
AVAILABILITY
Full Time
Skills
ADaM
Argus Safety
CDISC Standards
Clinical Reporting Tools
MedDRA
Metadata Documentation
MS Office
SAS
SDTM
TLF
WHO Drug Dictionary
Work Experience
Senior Statistical Programmer
Novartis
May 2022 – Present
- Develop and validate ADaM, SDTM, and TLF deliverables for clinical studies.
- Program analysis datasets and statistical reports ensuring accuracy, consistency, and documentation compliance. Collaborate with project teams to define specifications and deliverables within timelines.
- Contribute to pooled analyses and maintain metadata documentation to support regulatory requirements.
TECHNOLOGIES
SAS, SDTM, ADaM, TLF, CDISC Standards, Metadata Documentation
Statistical Programmer-II
Bayer
October 2018 – May 2022
- Programmed and validated SDTM/ADaM datasets and TLF outputs in compliance with study and regulatory standards.
- Supported study teams in data analysis and representation. Mentored junior programmers, ensuring adherence to company programming guidelines and best practices.
TECHNOLOGIES
SAS, ADaM, SDTM, TLF, CDISC, Clinical Data Standards
Operations Specialist
QuintilesIMS
October 2013 – March 2017
- Processed and coded SAE and AE reports according to global standards.
- Authored medical narratives, managed regulatory submissions, and performed QC of case reports.
- Conducted reconciliations and case closures to ensure data completeness and compliance.
TECHNOLOGIES
Argus Safety, WHO Drug Dictionary, MedDRA, MS Office, Clinical Reporting Tools
