Ousmane Diallo, MPH-PhD
Biostatistics & Epidemiology Solutions for Clinical Research
Iām Ousmane Diallo. I develop statistical models, regulatory-compliant workflows, and data analytics solutions to accelerate discovery in pharmaceutical and clinical research. My work integrates biostatistics, epidemiology, and CDISC standards to deliver insights for clinical trials and regulatory submissions.
With a background in epidemiology, biostatistics, and SAS clinical programming, I specialize in building CDISC-compliant solutions that accelerate pharmaceutical research. My work bridges statistical analysis, regulatory standards, and real-world evidence, supporting both academic research and industry applications.
About Ousmane Diallo
Ousmane Diallo is a rigorous biostatistician and epidemiologist specializing in health data analytics, statistical modeling, CDISC standards, and real-world evidence (RWE). With over 9 years of experience, he collaborates with academic researchers, pharmaceutical teams, and international health organizations to design regulatory-compliant analyses, reproducible workflows, and evidence-based solutions. His work connects biostatistics with clinical research and regulatory science, supporting discovery in both academia and industry.
Core Competencies
Programming & Tools
- SAS (Certified Base & Clinical Trials)
- R Programming (tidyverse, survival, spatial)
- Python ā¢ Quarto ā¢ GitHub
- Tableau & Power-BI
Clinical & Regulatory Standards
- CDISC: SDTM, ADaM & define.xml
- Clinical Trials Programming
- Statistical Analysis Plans (SAPs)
- GCP/ICH Compliance & Validation
Statistical & Analytical Methods
- Advanced Statistical Modeling (GLM, Survival)
- Real-World Evidence (RWE)
- Geospatial Analysis & Visualization
- Complex Survey Data Analysis
Professional & Collaborative Skills
- Cross-Functional Team Collaboration
- International Project Management
- Training & Mentorship Programs
- Quality Control & Data Validation
Professional Credentials
- š Certified SAS Base Programming & Clinical Trials Programming
- āļø 9+ Years Experience in Health Data Analytics & Statistical Modeling
- š§¬ CDISC Implementation Expert with proven regulatory submission experience
- š International Collaboration across Guinea, Burkina Faso, Togo, Benin
Key Projects & Achievements
- š Developed end-to-end CDISC workflows for regulatory submissions in pharmaceutical research
- šø Led geospatial analysis projects for malaria surveillance and intervention targeting across West Africa
- š¦ Implemented statistical modeling pipelines for real-world evidence studies and observational research
- š Open-source workflows and reproducible analyses available on GitHub
Ready to accelerate your clinical research with regulatory-compliant insights?
š Contact Me to discuss collaborations or consulting opportunities.
My Transition to Pharma/Industry
My academic background in epidemiology and biostatistics, combined with hands-on SAS training and CDISC projects, has prepared me to contribute to clinical trials and RWE studies. Projects like my end-to-end CDISC workflow (SDTM/ADaM, TLF, define.xml) demonstrate my ability to deliver regulatory-compliant deliverables, while my R-based analyses showcase transferable skills for RWE and observational studies.
Available for: Clinical Biostatistician ā¢ Statistical Programmer ā¢ Data Scientist roles
Frequently Asked Questions
What types of projects do you specialize in?
I specialize in clinical research projects, collaborating with pharmaceutical companies, academic institutions, and health organizations. My expertise includes CDISC implementation, statistical analysis for clinical trials, real-world evidence studies, and regulatory submission support across both industry and academic settings.
What kind of data do you analyze?
As a biostatistician and epidemiologist, I work with clinical trial data, real-world evidence datasets, health surveillance data, and complex survey data requiring advanced statistical methods for analysis. I also develop CDISC-compliant datasets (SDTM/ADaM) and create regulatory submission packages. I work at all stages of the research process, from study design to final reporting.
Do you offer training or consulting?
Yes! I provide mentorship and consulting in biostatistics, SAS programming, and CDISC standards for students and research teams. I also offer training in clinical trials programming, statistical analysis plans, and regulatory compliance workflows.
Where are you based and available for work?
I am actively seeking clinical biostatistician and statistical programmer positions in the pharmaceutical industry. Iām available for remote work and relocation opportunities worldwide, with experience in international collaborations.
Quick Facts
| Attribute | Detail |
|---|---|
| Name | Ousmane Diallo |
| Specialization | Biostatistics, Epidemiology, CDISC Standards |
| Experience | 9+ years in health data analytics & statistical modeling |
| Certifications | SAS Base Programming & Clinical Trials Programming |
| Industry Focus | Pharmaceutical, Clinical Research, Regulatory Science |
| Skills | SAS, R, Python, CDISC (SDTM/ADaM), Statistical Modeling, RWE |
| Availability | Seeking clinical biostatistician & statistical programmer roles |
| Portfolio | View Projects |