Own study deliverables quality and timeliness from startup through documentation filing
Report study issues and monitoring metrics proactively to global and country leadership
Oversee monitoring quality and meet recruitment targets for assigned clinical studies
What they want
Proven experience overseeing operational delivery across all clinical trial stages
Solid knowledge of clinical development processes and international ICH-GCP guidelines
Basic GMP and GDP knowledge with comprehensive current regulatory GCP knowledge
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Nice to have
Experience working with remote collaborators in matrix reporting structures
Manages change positively and treats change as performance improvement opportunity
Prioritizes multiple conflicting deadlines while staying team oriented and flexible
Seoulstart's read
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
Alexion Seoul clinical ops role; expect heavy local EC/CA,site contracts,and Korean regulatory interfaces even though Korean is not listed.
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.