Veronia Todary

With over a decade of experience managing global clinical programs and regulatory strategies, I help pharmaceutical and biotech companies accelerate their studies, secure approvals, and optimize vendor performance.

My dual expertise in Clinical Trial Management (Phases I–IV) and Regulatory Affairs (EMA/FDA submissions, compliance, inspections) allows me to bridge science, operations, and regulations to deliver results in high-stakes environments.

- Proven track record in oncology, hematology, and rare diseases

- Leadership in vendor negotiations (CROs, labs) and budget optimization

- Strong knowledge of ICH-GCP, EMA, FDA and international regulatory frameworks

- Experienced in rescuing delayed studies and aligning global stakeholders

If you’re looking for a hands-on senior consultant to drive your trial forward, solve complex regulatory challenges, or secure operational excellence, let’s connect.