Moving from discovery to a trial is a data problem as much as a science problem.
Bridgid Advisory helps biotech and digital health-tech teams build the data systems that make their evidence hold up, from endpoint design through submission. Most early-stage teams choose to design their data collection around the biology, only to find out too late their selection will not survive regulatory scrutiny.
That is the gap I bridge.
What does this study actually need in order to produce data that defends your science?
The answer is always specific. The work is always rigorous.
Research Sponsors building or improving EDC infrastructure
Contract research organizations (CROs) scaling operations and study startup
Clinical technology ventures (digital health-tech & wearable startups) building evidence for their interventions
Who I Work With
Every engagement draws on the same foundation: deep expertise in the systems that make clinical data defensible. Below you'll find the areas I focus on, and the ways we can work together. Whatever you need, we start with what your study actually requires.
Every engagement starts with one question
What I Do
How I Work with You
I help biotech and clinical-tech teams build the data systems that hold up their evidence, from endpoint design through submission.
Where I focus: endpoint and eCOA data, sensor and wearable data integrity, and trial data architecture built for submission.
How we start: most teams begin with a Gap Assessment, that shows exactly where data are vulnerable and what to fix.
Services - Where I Focus.
Endpoint Data Design.
Sensor & Wearable Data Integrity.
Trial Data Architecture.
Continuous sensor data generates gaps, outliers, and device failures that regulators will ask you to account for. I build the QC framework that documents what happened to your data, and why, before anyone asks.
Before your trial starts, you need a data plan designed for submission, not just collection. I align your data standards, vendor setup, and documentation to CDISC and 21 CFR Part 11 from the outset.
When your trial captures patient-reported or clinician-rated outcomes, the system behind the data matters as much as the instrument. I design, implement, and oversee eCOA systems so your outcome data is clean, auditable, and defensible.
■ Bridge ■ Identity ■ Data ■
Ready to Talk?
If you're dealing with research data challenges, and want to explore whether I can help, let's talk over your team's needs.
Select here to Book an Intake:
Or if no intake needed and urgent triage required for your team's needs,
Select here to Book a Consultation: