Clinical Research Associate I - II

As a CRA, you will play a key role in managing and monitoring clinical trials, ensuring compliance with regulatory requirements, and fostering strong relationships with investigative sites. This is a fantastic opportunity for professionals looking to grow their career in a dynamic and collaborative environment.Key ResponsibilitiesConduct site monitoring visits and ensure adherence to protocols and regulatory guidelines.Support site selection, initiation, and close-out activities.Collaborate with cross-functional teams to ensure study timelines and quality standards are met.Provide mentorship and guidance to junior CRAs as needed.QualificationsMinimum of 1 years of independent monitoring experience.Strong knowledge of ICH-GCP and local regulatory requirements.Excellent communication and organizational skills.Fluency in Korean and proficiency in English.Employment Type: Full-time, Hybrid workingIf you're ready to take the next step in your clinical research career, we’d love to hear from you!Learn more about our EEO & Accommodations request here.