Bilingual Pharmacovigilance and Medical Information Specialist with hands-on experience in global post-marketing safety operations, case processing, and translation (French–English). Skilled in handling medical and product quality inquiries, documenting safety data from multiple sources, and maintaining compliance with international regulations (ICH-GCP, EMA, FDA). Adept at collaborating with healthcare professionals, medical reviewers, and cross-functional safety teams to ensure patient safety and data accuracy. Adaptable and eager to expand expertise across lifecycle safety service lines.