Manage post-marketing regulatory commitment and real-world evidence study programs
Lead regulatory commitment studies from planning through clinical study report completion
Develop and maintain protocols,statistical analysis plans,and clinical study reports
What they want
Hold MS in life sciences,pharmacy,epidemiology,biostatistics,or related field
Bring two plus years pharma post-marketing,NIS,RWE,or regulatory commitment experience
Demonstrate advanced medical writing for protocols,CSRs,regulatory documents,and manuscripts
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Visa tier (likely)
F-2 / F-4 / F-5 / F-6 holders welcome
Korean language
Korean not required
English friendliness
High: JD in English, foreign-friendly signals
Context
Global pharma Seoul office; expect MFDS interactions and local compliance work even without stated Korean requirement.
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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