De-risk your clinical roadmap
Helping startups move from prototype to validated product by building the behavioral evidence needed for regulatory approval and investor confidence.
Expand your team's technical capabilities
Providing expert-level study design and advanced data analysis (MRI, R, Python) to help research teams deliver high-impact results without the overhead of additional full-time staff.
Turn lived experience into measurable impact
Translating the needs of your community into rigorous research frameworks that drive funding, policy change, and better clinical care.
For HealthTech
In the high-stakes environment of HealthTech, the gap between a prototype and a market-ready solution is built on evidence. I help you bridge that gap by ensuring your behavioral and clinical strategies are robust enough for regulators and intuitive enough for patients.
Can your adult-focused intervention scale to adolescents? I design the mechanism of action studies (like my PLAY project) to prove your solution works across demographics.
I identify the psychological friction points causing user churn and redesign protocols to optimize long-term treatment adherence.
From pilot studies to full clinical protocols, I ensure your data collection meets the standards required for FDA/EMA digital health submissions.
For Academics
As a fellow researcher, I understand the pressure of managing multi-site trials and complex data pipelines. I provide high-level technical support that allows your team to maintain scientific rigor and meet publication deadlines without the overhead of additional permanent staff.
Expert-level analysis of fMRI (FSL/SPM), psychophysiological markers (SCR/Cortisol), and behavioral datasets in R, Python, and Matlab.
I help you design studies that are scientifically rigorous but clinically feasible, reducing the risk of data loss in difficult-to-recruit pediatric or chronic pain populations.
Leveraging my track record of 15+ peer-reviewed publications to assist with high-impact manuscript preparation, systematic reviews, or ERC/FWO/NIH grant development.
For Patient Groups & Non-profits
Data is one of the most powerful tools in advocacy. I help patient-led organizations and non-profits bridge the gap between lived experience and scientific evidence, creating the robust foundations needed to drive funding, policy change, and better clinical care.
I help you turn community insights into measurable data. By structuring surveys and qualitative studies with scientific rigor, I ensure your organization’s claims are backed by publication-grade evidence.
I create accessible White Papers, Systematic Reviews, and "State of the Science" reports. These documents simplify complex neurobiology and health psychology into clear, persuasive arguments for stakeholders and policymakers.
I advise on how to design studies that are sensitive to the needs of your community. Using my clinical background, I ensure research protocols are trauma-informed and accessible for "hard-to-reach" or highly symptomatic groups.