Clinical Research Associate 2

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](https://careers.fortrea.com/us/en/eeo-and-accommodations).