CMC Regulatory Expert Biopharma

Excelya · Paris, Île-de-France, France

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Entreprise
Excelya
Lieu
Paris, Île-de-France, France
Type de contrat
Temps plein
Publiée le
2 juin 2026

À propos de ce poste

At Excelya, we are committed to fostering an environment defined by Audacity, Care, and Energy. As a Clinical Operations Lead, you will play a vital role in enhancing our clinical research strategies and ensuring operational excellence across our studies. This position offers a unique opportunity to lead strategic CMC regulatory initiatives while collaborating with cross-functional stakeholders to ensure the highest standards of quality and compliance. You will play a key role in driving regulatory excellence, supporting complex global submissions, and contributing to innovative development and lifecycle management strategies that shape the future of medicines. Main responsibilities: Define and lead the CMC regulatory strategy for complex projects, providing proactive guidance and expertis

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