Alpha S. Traoré
Principal Statistical Scientist
I’m Alpha S. Traoré, a Principal Statistical Scientist with 9+ years supporting Phase I–III clinical development. I turn complex trial data into traceable, submission-ready analyses across oncology, rare disease, and PK/PD.
Principal Statistical Scientist
About me
My work sits at the intersection of biostatistics, statistical programming, and clinical data strategy.
I transform complex trial data into dependable datasets, tables, listings, figures, and analytical tools. My experience spans Phase I–III clinical development, selected preclinical studies, oncology, rare disease, PK/PD, and integrated submission work, including NDA, ISS, and ISE deliverables.
I care about traceability, thoughtful validation, and process improvement. I develop reproducible analyses, analytical applications, and AI-enabled tools that strengthen data quality and support confident decisions—not just code that runs.
Expertise
From raw clinical data to validated evidence and decision-ready reporting.
Analysis datasets, TLF development, validation, reusable macros, and regulatory-ready production workflows.
Traceable implementation of CDISC standards supporting consistent analysis and regulatory review.
Clear analytical reasoning for clinical endpoints, patient characteristics, and complex research questions.
Reproducible applications and AI-enabled tools that improve data quality, streamline workflows, and make complex results easier to review and communicate.
Experience
Progressive responsibility from hands-on biostatistics to principal-level scientific leadership — 2017 to present.
BioSTAT Consultants Inc.
Promoted from Senior to Principal in 2026. Sets statistical strategy across 8 active programs, from study design through regulatory submission, and leads a cross-functional programming team—after two years owning end-to-end biostatistics and programming for 10 studies.
Precision for Medicine
Built CDISC-compliant SDTM and ADaM pipelines and TLFs across 20+ studies in oncology and rare disease, including PK programming and integrated ADaM datasets for ISS/ISE in an NDA submission.
BioSTAT Consultants Inc.
CTI Clinical Trial & Consulting Services
PPD
Built a foundation in biostatistics across three organizations—authoring SAPs, ADaM specifications, and ISS/ISE datasets for NDA submissions, and leading cross-functional teams of 4–8 on Phase I–III studies.
Selected work
Four technical projects spanning oncology analytics, statistical science, CDISC implementation in R, and interactive clinical-data workflow design.
An end-to-end R workflow that transforms synthetic patient demographics, diagnoses, and treatment records into analysis-ready clinical insights.
A comprehensive technical library connecting study strategy, estimands, modeling, SDTM, ADaM, TLFs, validation, and submission-readiness.
Supporting notebooks from a CDISC Pediatric User Network presentation, demonstrating synthetic DM inputs, SDTM mapping, and ADSL creation.
A functional portfolio prototype connecting aCRF annotation, SDTM and ADaM specifications, statistical programming, TLF development, traceability, validation findings, and submission readiness.
Certifications
Industry-recognized certifications from Certara, SAS, and CDISC.
View verified credentials
Certara

Certara

Certara

SAS

CDISC
Let’s connect
I’m always interested in thoughtful conversations about clinical statistics, programming, and data-driven research.