About this role
Safety Specialist II at Precision Medicine Group. Location: Serbia. Role: processing reports, entering data, coding events Requirements: 2+ years clinical trial drug safety experience, experience with Oracle Argus, working knowledge of MedDRA and WHODrug, familiarity with global safety regulations (FDA, EMA, MHRA, ICH). Bachelor's in pharmacy, nursing, or life science preferred. Category: Research and Development (R&D) Seniority: Entry Level Tools: Oracle Argus Safety Database, MedDRA, WHODrug Commitment: Full Time Workplace: Remote Languages: English