A leading pharmaceutical company in Italy is seeking a Start Up Specialist to oversee regulatory submissions and act as the primary contact for investigative sites. The ideal candidate will have at least 3 years of experience in clinical study start-up and regulatory affairs, coupled with a solid understanding of ICH-GCP guidelines. The role involves preparing regulatory applications, ensuring compliance, and managing communication with stakeholders. Excellent organizational skills and the ability to manage multiple projects are essential for success in this position.#J-18808-Ljbffr