Clinical Safety Coordinator

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.