Teams at Arriello Ireland Limited

Manage regulatory activities for pharmaceutical and biotechnology client projects, focusing on clinical trial applications and early development submissions. Prepare and submit dossiers using CTIS, eCTD, IRAS, and related formats; support Scientific Advice, PRIME, ODD, and Early Access Programme pathways. Coordinate documentation, translations, labeling, compliance, audits, and regulatory intelligence while collaborating with clients, health authorities, vendors, and internal teams.