Lead moderate-to-high complexity clinical studies independently per GCP and contracts
Manage clinical operations,quality,timelines,and deliverables for allocated studies
Develop monitoring plans,guidelines,and Trial Master File sections on time
What they want
Eight plus years comparable clinical trial management experience required
Recent hematology and oncology clinical experience is mandatory
Bachelor's degree or equivalent relevant formal qualification required
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Nice to have
Regional lead CTM or Clinical Study Manager responsibilities experience preferred
Dose escalation,cohort basket,and master protocol study experience preferred
Phase one and three regional global study experience preferred
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
Seoul base for APAC HemOnc CRO work at a global sponsor; expect frequent domestic site travel and English-led client calls.
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.