Oversees,designs,plans,and develops clinical evaluation research studies
Prepares and authors clinical protocols and patient record forms
Conducts registered and non-registered clinical studies for medical products
What they want
Bachelor's plus four years relevant experience,or advanced degree plus two
Medical device or pharmaceutical industry clinical research experience required
Excellent communication skills and stakeholder relationship management
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Nice to have
Preferably seven years of relevant clinical research setting experience
Practical project management knowledge for clinical trial oversight work
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
Global medtech Seoul role with local GCP and regulator-facing work; Korean may still help with sites and authorities though unstated.
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.
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