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This is one hour of one-on-one consultation for a nonprofit organization, booked directly with me, on whatever research or data problem you're working through.
Some of the topics people bring to these calls:
Structuring a natural history study or patient registry
Working with electronic health records or the OMOP common data model
Planning a rare disease research project, from study design through data collection
Real world evidence approaches for a specific drug, condition, or population
Building or interpreting a computable phenotype
Preparing materials for an FDA listening session or patient-focused drug development meeting
Advocacy group strategy: what a registry, database, or research partnership can realistically do for your organization
General guidance on getting a nonprofit, grant writing, data science, or biomedical informatics project off the ground
You don't need a fully formed question to book a session. Bring a problem, a data set, a protocol draft, or just a general direction, and we'll work through it together.
What happens after you book
You'll receive a scheduling link to pick a time that works for you
A short intake form asks what you'd like to cover, so I can prepare
We meet for one hour over video call
You'll get a follow-up email with notes and any resources mentioned during the call
Fine print
Sessions are booked in one-hour increments; longer engagements can be arranged separately
This consultation is educational and advisory. It does not constitute medical, legal, or regulatory advice
Cancellations require [X hours/days] notice for a reschedule
This is one hour of one-on-one consultation for a nonprofit organization, booked directly with me, on whatever research or data problem you're working through.
Some of the topics people bring to these calls:
Structuring a natural history study or patient registry
Working with electronic health records or the OMOP common data model
Planning a rare disease research project, from study design through data collection
Real world evidence approaches for a specific drug, condition, or population
Building or interpreting a computable phenotype
Preparing materials for an FDA listening session or patient-focused drug development meeting
Advocacy group strategy: what a registry, database, or research partnership can realistically do for your organization
General guidance on getting a nonprofit, grant writing, data science, or biomedical informatics project off the ground
You don't need a fully formed question to book a session. Bring a problem, a data set, a protocol draft, or just a general direction, and we'll work through it together.
What happens after you book
You'll receive a scheduling link to pick a time that works for you
A short intake form asks what you'd like to cover, so I can prepare
We meet for one hour over video call
You'll get a follow-up email with notes and any resources mentioned during the call
Fine print
Sessions are booked in one-hour increments; longer engagements can be arranged separately
This consultation is educational and advisory. It does not constitute medical, legal, or regulatory advice
Cancellations require [X hours/days] notice for a reschedule