Clinical Research Associate II

<p>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.</p><p></p><p><b>Key Responsibilities:</b></p><ul><li><p>Conduct site monitoring visits and ensure adherence to protocols and regulatory guidelines.</p></li><li><p>Support site selection, initiation, and close-out activities.</p></li><li><p>Collaborate with cross-functional teams to ensure study timelines and quality standards are met.</p></li><li><p>Provide mentorship and guidance to junior CRAs as needed.</p></li></ul><p></p><p><b>Qualifications:</b></p><ul><li><p>Minimum of 1.5 years of independent monitoring experience.</p></li><li><p>Strong knowledge of ICH-GCP and local regulatory requirements.</p></li><li><p>Excellent communication and organizational skills.</p></li><li><p>Fluency in Korean and proficiency in English.</p></li></ul><p></p><p><b>Employment Type:</b> Full-time, Hybrid working</p><p></p><p>If you&#39;re ready to take the next step in your clinical research career, we’d love to hear from you!</p><p></p><p><span>Learn more about our </span><a href="https://careers.fortrea.com/us/en/eeo-and-accommodations" target="_blank">EEO &amp; Accommodations request here</a><span>.</span></p>