Clinical Safety Coordinator - Pharmacovigilance (Nursing Professionals Encouraged to Apply)

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. Responsibilities - 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; - Process clinical trial and post marketing serious adverse events - Translate safety documents between Korean and English; - Track, process, and organize various safety-related documents; - Perform other duties as assigned by the Clinical Safety department Qualifications - Degree in Life Science - Minimum 2 years of relevant Pharmacovigilance experience - Strong attention to detail and communication skills Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. Why Medpace? When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.   Purpose-Driven Work - - Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence   Collaborative Culture - - Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. - Leadership throughout Medpace is both accessible and approachable   Continuous Growth & Development - - Office based environment with on-site mentors - Defined career paths with clear advancement opportunities - Industry renowned onboarding and training programs designed to accelerate professional development - Ongoing training and continuous learning opportunities throughout your career - An environment that encourages employees to influence change, contribute ideas, and grow quickly   Other Employee Benefits - - Competitive compensation programs that recognize and reward performance - Comprehensive health, wellness, retirement, and PTO benefits - Office based culture with occasional WFH that provides flexibility for eligible positions after training - Company-sponsored social events    Please note benefits may vary based on country.      What to Expect Next A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted. - 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; - Process clinical trial and post marketing serious adverse events - Translate safety documents between Korean and English; - Track, process, and organize various safety-related documents; - Perform other duties as assigned by the Clinical Safety department - Degree in Life Science - Minimum 2 years of relevant Pharmacovigilance experience - Strong attention to detail and communication skills