Senior Clinical Operations/Clinical Science Consultant with 25+ years of experience delivering clinical trials across all phases of research. Deep expertise managing complex global IDE/IND studies, driving study design, operational execution, vendor and site oversight, and cross‑functional leadership. Proven track record managing studies from concept through CSR in compliance with FDA, EU MDR, and ICH‑GCP requirements. Recognized for strategy, financial stewardship, and building strong partnerships with investigators, vendors, and internal and external stakeholders.
Member Since
February 19, 2026
Last Active
4 months ago