Safety Associate (1-Year Contract)
IQVIA · Seoul, South Korea
SafetyFull-timeCompany career page
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Role summary
IQVIA seeks a Safety Associate for a one-year contract role in Seoul to review, process, and distribute pharmacovigilance data and adverse event information across service lines while maintaining compliance with regulations and quality standards.
What they're looking for
- Bachelor's degree in scientific, healthcare, or allied life sciences discipline
- 1-1.5 years of relevant safety or pharmacovigilance experience
- Knowledge of medical terminology and applicable safety databases
- Understanding of global, regional, and local clinical research regulatory requirements
- Proficiency in Microsoft Office and web-based applications
- Strong organizational, time management, and written communication skills
- Ability to work independently, multitask, and manage competing priorities
What you'll be doing
- Process safety data according to regulations, SOPs, and project requirements
- Collect, track, and assess incoming adverse events and endpoint information; perform database entry and medical coding
- Write narratives and conduct literature-related activities per project timelines
- Create, maintain, and track cases while identifying quality issues and escalating to senior team members
- Attend project meetings, provide operational feedback, and mentor new team members as assigned
Privacy & handoff
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