Proven experience in clinical development strategy, including design of efficient development programs, CDPs, and study protocols, as well as support of indication and territory expansions * 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 * 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 * Medical doctor (MD), pharmacist, or equivalent life sciences degree with ideally five years of international clinical research experience (Phase I–III) * Experience with regulatory interactions and submissions (EMA and / or FDA), with strong knowledge of GCP/ICH and applicable regulations
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