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Clinical Safety Coordinator

Full-Time Seoul, South Korea
Health & Biotech
Health & Biotech
20 June 2025
Description
  • Work closely with the Clinical Safety Manager to ensure project deliverables are met;
  • Generate safety letters as applicable and submit SUSAR reports and aggregate reports to the regulatory authority in South Korea;
  • Conduct quality control review of safety reports and other department documents as needed;
  • Translate safety documents between Korean and English;
  • Track, process, and organize various safety-related documents;
Qualifications
  • Minimum 2 years of relevant Pharmacovigilance experience.
  • Strong attention to detail.

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