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 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.