I lead global clinical trials from start-up to delivery, managing timelines, budgets, vendors and stakeholders while maintaining focus on execution, quality, compliance and inspection readiness.
When programs grow in complexity, I stay close to what drives delivery — decisions are clearer, priorities stay aligned, and studies keep moving.
I support study planning, start-up and execution, translating development plans into operational reality with realistic timelines, budgets and risk awareness from the beginning.
This reduces friction later and allows studies to move into execution with fewer gaps.
I work with CROs and vendors to set expectations, monitor delivery and address issues early, keeping accountability clear across the study.
This helps protect timelines and prevents operational issues from escalating.
I plan and support investigator meetings, from agenda and content to delivery and facilitation.
Well-structured meetings support engagement, clearer alignment and stronger study start-up.
I help companies prepare for due diligence based on experience from both sides of the process, identifying gaps early and preparing teams for discussions with partners and investors.
This makes the process more structured, predictable and easier to navigate.
Whether you're building infrastructure for a first-in-market trial, recovering a program that's drifted off course, or integrating teams across cultures that don't naturally align — start with a conversation.
