Job description
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!
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