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.
Top Skills
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
