Proven track record in designing smart, integrated clinical development programs, evaluating new assets through due diligence, and advancing lifecycle strategies, including indication extensions and territory expansions * Lead global clinical development programs across Phase I–III trials, overseeing multiple studies and ensuring high-quality execution, data integrity, and timely delivery * Design and drive efficient, integrated clinical development strategies, including Clinical Development Plans (CDPs) and Target Product Profiles (TPPs), aligned with scientific, regulatory, and commercial objectives * Oversee development and quality of core clinical and regulatory documents, ensuring consistency and scientific rigor across all deliverables * Proven experience in clinical development strategy, including design of efficient development programs, CDPs, and study ...
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