Represent Korea Medical Affairs and collaborate with global/regional and cross-functional partners (Clinical, RA/QA, Marketing, FIN, Supply chain etc.)
Drive policy/process development and operational excellence
Build and manage annual medical plans, budgets, and resources
Lead people development, coaching, performance management, and staffing
2. Clinical Evidence Generation & Research Management
Provide medical review and ensure quality/compliance for local/global clinical studies and pre-market studies
Review study documents (Protocol, CRF, ICF, etc.) and ensure compliance with regulations, BSC SOPs, and GCP
Lead communications with investigators/sites to monitor study progress and resolve issues
Secure and manage essential resources (investigators, institutions, documentation, budget, vendor/site contracts, material resources) required for participation in pre‑market or global clinical studies; proactively identify timelines/risks and implement mitigation
3. HCP Scientific Program & Internal Education/Consultation
Provide therapeutic/product scientific consultation based on current evidence
Plan and deliver HCP engagement programs and up-to-date safety/clinical use information
Provide internal medical training (product knowledge, clinical data updates)
4. Medical Compliance & Quality
Ensure compliance with regulations, BSC Quality Policy, and SOPs across all medical activities
Lead audit responses and CAPA activities
Own medical review for ethics and promotional/advertising materials
5. External Engagement & KOL partnership
Strengthening KOL and institutional networks
Plan and lead advisory boards, symposia, and scientific engagement activities
[Required Qualifications]
Bachelor's degree in life sciences or related field
Fluent in English, with the ability to communicate effectively across global and regional stakeholders
15–20 years of experience in Medical Affairs, Clinical Research, or related areas, including a minimum of 3 years of people and team management experience
Strong cross-functional communication and stakeholder management
Demonstrated people leadership
[Preferred Qualifications]
Advanced degree (Master, PhD) in Medicine (MD, MSc), Biomedical Sciences (MSc/PhD in Biomedical Science), Life
Sciences (MSc/PhD in Physiology), Public Health / Epidemiology (MPH, MSc in Epidemiology)
Experience in global clinical research, including Korea’s participation in pre-approval trials
Deep understanding of MedTech/pharma regulations, GCP, clinical trial processes, and data integrity
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