Safety Associate (Pharmacovigilance)

Location: Seoul, Republic of Korea

Company

Global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Process safety data and information from multiple sources according to regulations, SOPs, guidelines, and project requirements.
• Collect, track, assess, and maintain adverse event and endpoint information.
• Determine initial or follow-up event status, enter data into safety databases, and code adverse events and products.
• Write case narratives and support literature-related pharmacovigilance activities within project timelines.
• Monitor quality, productivity, delivery, and compliance standards, escalating issues to senior team members.
• Attend project meetings, provide operational feedback, and mentor new team members when assigned.

Requirements

• Bachelor’s degree in a scientific, healthcare, or allied life sciences discipline.
• 1–1.5 years of relevant experience.
• Knowledge of medical terminology, safety databases, and global, regional, and local clinical research regulations.
• Strong attention to detail, accuracy, organization, time management, and communication skills.
• Ability to follow procedures, work independently, manage competing priorities, and meet deadlines.
• Flexibility to work shifts and sit for extended periods; occasional travel may be required.

Culture & Benefits

• Full-time work with a one-year contract.
• Structured training across safety service lines.
• Collaboration with coworkers, managers, clients, and project teams.
• Work is guided by defined quality, productivity, delivery, and compliance standards.