Protect subject rights while verifying accurate,complete,verifiable study data
Perform and coordinate clinical monitoring independently across assigned sites
What they want
Hold university degree in nursing or life sciences field
Have one year independent on-site pharma or CRO monitoring experience
Demonstrate understanding of ICH-GCP,MFDS,and FDA requirements
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Seoulstart's read
Visa tier (likely)
E-7 specialty / professional (likely)
Korean language
Korean not required
English friendliness
High: JD in English, foreign-friendly signals
Context
Remote Korea CRA on GSK-sponsored trials; MFDS regulatory knowledge is explicitly required.
This is Seoulstart's analysis of the public job description, not the employer's stated policy. Verify visa sponsorship, language requirements, and remote allowances directly with the recruiter.