Projects

Projects

Pharmacoeconomic Policy Model

Developed cost-effectiveness models to evaluate high-cost drug therapies, influencing payer reimbursement policies in the US healthcare system.

2023 – Present

Pharmacoeconomic Policy Model
Epidemiology & Public Health Study

Led a large-scale epidemiological survey analyzing disease prevalence in underserved populations, creating data pipelines for public health interventions.

2015 – 2017

Epidemiology & Public Health Study
Microbiome & Heart Health

Investigated the link between oral bacteria and heart risks (obesity & hypertension) in adolescents, identifying early predictive markers.

2020-2021

Microbiome & Heart Health
Smokeless Tobacco Epidemiology

Conducted a cross-sectional study on smokeless tobacco consumption among heavy-load drivers, highlighting cancer risks in underserved communities.

2017

Smokeless Tobacco Epidemiology
OHIP-14 Quality of Life Model

Validated the 'Oral Health Impact Profile' (OHIP-14) for patients with liver and GI disorders, creating a new standard for measuring patient well-being.

2018

OHIP-14
Global Systematic Reviews

Conducted comprehensive meta-analyses on clinical datasets to generate high-level evidence for medical guidelines and treatment protocols.

2019-2022

Global Systematic Reviews
Pharmacoeconomic Policy Model

Developed cost-effectiveness models to evaluate high-cost drug therapies, influencing payer reimbursement policies in the US healthcare system.

2023-Present

Pharmacoeconomic Policy Model
Sanofi Market Access

Directed a $15M rare disease portfolio, driving 50% revenue growth for key therapies.

2021-2022

Sanofi Market Access
MammoCheck Strategy

Designed U.S. market entry strategy, accelerating speed-to-market by 40% with $50M+ projected revenue.

2023-2024

High-Tech Corporate Strategy
Gastro-Dental AI Analytics

Leveraged machine learning on national datasets to decode the link between oral health and gastrointestinal diseases.

2019-2021

Gastro-Dental AI Analytics
COVID-19 AI Diagnostics

Achieved >90% predictive accuracy using AI models, reducing diagnostic costs by 60%

2020-2021

AI Speed
Fabry Disease PRO Instrument

Developed a validated patient-reported outcome measure to support global drug launch evidence.

2022-2023

Fabry Disease PRO Instrument
Microbiome & Heart Health

Investigated the link between oral bacteria and heart risks (obesity & hypertension) in adolescents, identifying early predictive markers.

2020-2021

Microbiome & Heart Health
Salivary Biomarker Discovery

Pioneered non-invasive diagnostic models using salivary proteins to detect systemic diseases with high sensitivity.

2018-2020

Salivary Biomarker Discovery
Epidemiology & Public Health Study

Led a large-scale epidemiological survey analyzing disease prevalence in underserved populations, creating data pipelines for public health interventions.

2015-2017

Epidemiology & Public Health Study
Smokeless Tobacco Epidemiology

Conducted a cross-sectional study on smokeless tobacco consumption among heavy-load drivers, highlighting cancer risks in underserved communities.

2017

Smokeless Tobacco Epidemiology
Global Systematic Reviews

Conducted comprehensive meta-analyses on clinical datasets to generate high-level evidence for medical guidelines and treatment protocols.

2019-2022

Global Systematic Reviews
FAQ

Questions & Answers

What types of organizations do you partner with?

I work with a diverse range of clients, including top-tier Pharmaceutical Companies, Biotech Startups, Healthcare Systems, and Public Health Policymakers. Whether you need Global Market Access strategy or Clinical Validation, I tailor my approach to your specific scale and goals.

My methodology combines Real-World Evidence (RWE) with advanced Machine Learning models. This allows us to predict patient outcomes, optimize clinical trial designs, and reduce speed-to-market, ensuring that every strategy is backed by rigorous data analytics.

 

Yes. A key part of my work involves generating high-quality Health Economics & Outcomes Research (HEOR) data. I help structure scientific evidence and dossiers that align with regulatory requirements for bodies like the FDA and EMA to support successful product launches.

I offer flexible engagement models depending on your needs. This ranges from Project-Based Consulting for specific deliverables (e.g., a Market Entry Strategy) to Long-Term Advisory Retainers for ongoing scientific leadership and R&D support.

Data integrity is paramount. I adhere to strict global standards, including HIPAA and GDPR, ensuring that all patient data and proprietary client information is handled with the highest level of security and confidentiality throughout the project lifecycle.

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