We are currently seeking a full-time, experienced Clinical Research Associate to join our Clinical Operations team in the South Korea 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. Our culture is of expertise, and we empower our teams to employ their unique talents and experience to take an assertive approach to research, problem solving, and ultimately supporting our business partners. At Medpace, our employees embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return they are rewarded with interesting projects, career advancement, and recognition and exposure to our international footprint. These are just a few reasons why talented individuals join the Medpace team.

• Verify that the rights and well-being of subjects are protected, the reported trial data are accurate, complete, and verifiable from source documents, and the conduct of the trial is in compliance with the currently approved protocol/amendment(s), GCP, and applicable regulatory requirement(s); • Ensure site compliance while conducting qualification, study initiation, routine monitoring, and study site close-out visits for research sites according to Medpace/Sponsor Standard Operating Procedures (SOPs); • Serve as the primary resource to the clinical investigator and site staff; • Maintain close collaboration, interaction, and effective working relationships with Medpace internal cross-functional teams; and • Ensure quality completion of visit reports, follow-up letters, and maintenance of study-related databases and ClinTrak ® Monitoring Portal.

• Bachelor's degree in a health or science related field and with at least 1.5 to 5 years of experience in clinical monitoring; • Comprehensive knowledge of practices and procedures relating to all clinical monitoring visit types, including practical application of this knowledge; • Demonstrated ability to act as a Lead CRA (as applicable); Act as a resource for new CRAs and ability to facilitate training and serve as a mentor for new CRAs; and • Implements new ideas/solutions, without prompting, within their authority.