Maxime joined Cilcare after gaining experience in medical care licensing at Pierre Fabre and innovation valorization at CHU Montpellier. After starting in the Quality department, he moved into his current role as Junior Project Leader & Regulatory Manager, where he plays a transversal role across the company. Maxime drives the planning and coordination of drug development projects, from early design through regulatory submission of clinical trial applications (CTA/IND), ensuring compliance with timelines and budgets.

With a dual background in pharmacy (PharmD) and innovation management, he combines strong analytical skills with a collaborative mindset to advance Cilcare’s innovative therapies.