Global Regulatory Affairs Specialist

Social network you want to login/join with: Global Regulatory Affairs Specialist, Caserta Our client, Chiesi Farmaceutici – one of the top 50 pharmaceutical companies worldwide with over 80 years of experience in the pharmaceutical and biotechnology industry – is expanding its team. IQVIA is recruiting a Global Regulatory Affairs Specialist to join an dynamic, international environment. Position Details: Purpose: As a core member of the GRT and strategic partner of the GRL, leverage regulatory expertise to define and execute EU, extra-EU, and global regulatory strategies, ensuring alignment with business objectives. Main Responsibilities: Serve as regional/local regulatory lead, develop HA interaction strategies, manage engagement plans, oversee regulatory submissions, contribute to document content, support inspections, and provide project updates. Experience Required: Approximately 3 years in Regulatory Affairs. Technical Skills: Understanding of clinical development, LCM activities, experience with electronic document management systems like Veeva Vault, and ability to handle multiple projects. Soft Skills: Stress management, time management, planning, organizational skills, and strategic thinking. What We Offer: Competitive salary Permanent contract Chemical contract IQVIA reserves the right to evaluate candidates based on domicile, residence, work experience, and studies. Applications lacking the required qualifications will not be fully considered. Consent for data processing is required as per GDPR regulations. The position is open to candidates of all genders. J-18808-Ljbffr

Location: caserta, IT

Posted Date: 6/16/2025