Ensure site studies follow approved protocol,ICH GCP,client standards,and laws
Protect subject rights and verify study data is accurate and source-verifiable
Perform and coordinate clinical monitoring,including independent on-site monitoring activities
What they want
Hold a university degree in nursing or another life-sciences field
Have at least two years of independent on-site monitoring at pharma or CRO
Demonstrate understanding of ICH-GCP,MFDS,and FDA regulatory 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 FSP CRA for a global CRO network; MFDS familiarity is explicit,Korean not stated.
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.