We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team in South Korea, Seoul office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company’s success. If you are interested in an exciting career where you can use your expertise and develop and grow your career even further, then this is the opportunity for you.

• 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;

• Minimum 2 years of relevant Pharmacovigilance experience. • Strong attention to detail.

For more details, please refer to the company website.