With 19 years of experience in clinical operations, I help small to mid-sized biotech companies accelerate global trials by combining deep site-focused expertise with AI-enhanced workflows and custom-built tools.
From oncology to rare diseases, I’ve specialized in study startup, patient recruitment, and retention—because success isn’t just about science; it’s about operational excellence at the site level.
My unique value lies in bridging two worlds:
📊 Clinical Trial Tools
💪 Patient Recruitment & Retention Strategy → DEI-aligned, patient-centered approaches that sustain enrollment.
🌍 Global Study Management & CRA Oversight → Leading teams across U.S., EU, APAC, LATAM with consistent quality, safety, and inspection readiness.
🤝 Diversity, Equity & Inclusion (DEI) Consulting → Building inclusive frameworks to ensure representative enrollment.
📑 Regulatory Navigation → Expertise in EUCTR, IVDR, and CDx integration to remove bottlenecks and enable timely site activation.
Consulting Rates 💵
My rates are designed to align with the needs of small-to-mid-sized companies looking for targeted, flexible expertise. Rates vary based on project scope and complexity. Below are my base rates for standard services:
| Service | Description | Suggested Hourly Rate (20+ yrs exp) |
|---|---|---|
| Patient Advocacy & Recruitment Strategist 💪🏾 | Crafting and executing community-centered recruitment & retention strategies; DEI-aligned outreach | $175–$200/hr |
| Global Study Management🌍 | Senior oversight of Phase I–IV global trials, vendor management, EUCTR/IVDR submissions, startup | $225–$275/hr |
| Senior CRA Services 🔬 | Hands-on monitoring, site management, data integrity review, inspection readiness | $150–$175/hr |
| Site Strategy & DEI Consulting 🫱🏾🫲🏼 | Building DEI frameworks, site tiering strategies, patient equity initiatives, decentralized trials | $175–$200/hr |