Clinical Research Associate 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 Responsibilities: Conduct 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. Qualifications: Minimum of 1.5 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 working If 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 .