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Zayan Qureshi
Senior Statistical Programmer
Results-oriented Senior Statistical Programmer with 8+ years of experience in clinical trial programming, statistical analysis, and data management. Skilled in developing ADaM, SDTM, and TLF datasets across oncology, immunology, and vaccine studies. Adept at regulatory submissions, process automation, and cross-functional collaboration. Proven leadership and mentoring abilities, with expertise in compliance (P21, 21 CFR Part 11) and advanced data visualization techniques.
FORMERLY AT
IQVIA
LOCATION
Banglore
AVAILABILITY
Full-time
Skills
21 CFR Part 11
ADaM
Advanced
CDISC
Clinical Data Repositories
GCP
GPP
Macros)
P21 Validator
R
R (Beginner)
SAS
SAS (Base
SDTM
SQL
Work Experience
Senior Statistical Programmer
IQVIA
Jul 2024 – Present
Served as Principal Programmer for a Phase 3 immunology study ensuring FDA compliance via P21.
Developed ADaM datasets (ADSL, BDS, OCCDS) and created efficacy and safety TLFs.
Designed metadata and advanced visualizations including KM, Forest, Swimmer, and Waterfall plots.
Supported PK/PD dataset creation and regulatory compliance (21 CFR Part 11) processes.
TECHNOLOGIES
SAS (Base, Advanced, Macros), SQL, R (Beginner),CDISC, SDTM, ADaM,SAS, R, P21 Validator, Clinical Data Repositories,GCP, GPP, 21 CFR Part 11
Senior Statistical Programmer
Merck
Sep 2022 – Jul 2024
Led programming for Phase 2/3 clinical studies; prepared metadata, mock shells, and DSUR reports.
Managed vendor deliverables, mentored junior programmers, and supported FDA submissions.
Built macros for process optimization and handled ML datasets for regulatory requests.
Served as POC for statistical programming at the India site, ensuring P21 compliance.
TECHNOLOGIES
SAS (Base, Advanced, Macros), SQL, R (Beginner),CDISC, SDTM, ADaM,SAS, R, P21 Validator, Clinical Data Repositories,GCP, GPP, 21 CFR Part 11
Statistical Analyst
Eli Lilly & Company
Aug 2020 – Sep 2022
Transformed raw data into SDTM and ADaM datasets using SAS Base/Macros.
Created SDTM specifications, conducted quality checks, and generated mock TLFs.
Worked on oncology endpoints such as PFS, OS, ORR, and DFS along with efficacy datasets (ADLB, ADTR, ADTTE).
Championed data quality initiatives and standard implementation.
TECHNOLOGIES
SAS (Base, Advanced, Macros), SQL, R (Beginner),CDISC, SDTM, ADaM,SAS, R, P21 Validator, Clinical Data Repositories,GCP, GPP, 21 CFR Part 11
Statistical Programmer
Tata Consultancy Services
Nov 2016 – Aug 2020
Delivered sponsor-specific data transformations for leading US pharmaceutical clients.
Developed SAS macros and programs for data mapping, analysis, and automation.
TECHNOLOGIES
SAS (Base, Advanced, Macros), SQL, R (Beginner),CDISC, SDTM, ADaM,SAS, R, P21 Validator, Clinical Data Repositories,GCP, GPP, 21 CFR Part 11
We handle the recruitment process, screening and shortlisting candidates.
therapeutic area, function, tools, time zone, start date.
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