Clinical Safety Coordinator

Responsibilities

• Work closely with the Clinical Safety Manager to ensure project deliverables are met
• Generate safety letters and submit SUSAR reports and aggregate reports to South Korean regulatory authorities
• Conduct quality control reviews of safety reports and other departmental documents
• Translate safety documents between Korean and English
• Track, process, and organize various safety-related documents

Requirements

• Minimum 2 years of relevant Pharmacovigilance experience
• Strong attention to detail
• Proficiency in translating documents between Korean and English

Benefits

• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Flexible work environment
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

About the Company

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. Headquartered in Cincinnati, Ohio, we employ more than 6,000 people across 40+ countries.