About this role
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.