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
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators.
Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas.
Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes.
Together, exceptional is possible.
Learn more at Fortrea.com
