Title:  Specialist Medical Science Liaison

[EXPERIENCE]
1. Industry Experience: Minimum 3+ years of professional experience in the pharmaceutical industry, specifically within Medical Affairs or Clinical Research.
2. Project Management: Extensive experience in managing the full life cycle of research projects, including budget projection and outsourced resource management.
3. Therapeutic Area: Expertise in communicating complex scientific information and managing stakeholder relationships within specific disease portfolios.

[JOB DESCRIPTION]
1. Medical Strategy & Scientific Engagement
• KOL Management: Develop and establish strong scientific peer-to-peer engagement with top-tier Key External Experts (KEE) and Key Opinion Leaders (KOL) to enhance the understanding of disease areas and product value.
• Strategic Input: Provide expert medical input into Government Affairs and Market Access activities to shape business strategy and brand value propositions.
• Support scientific exchange at local, regional, and international medical congreesses, advisory boards, symposia, and other scientific meetings
• Medical Training: Plan and organize scientific training for internal partners (e.g., sales force) and external stakeholders to ensure high-level medical knowledge.

2. Medical Insight Generation
• Systematically gather, analyze, document, and communicate actionable medical insights from external stakeholders and the healthcare environment 
• Identify unmet medical needs, evidence gaps, clinical practice challenges, access barriers, and emerging scientific trends 
• Contribute to the development and periodic refinement of the medical affairs strategy and field medical plan

3. Evidence Generation (PMS, IIS, & OS)
• Provide scientific and operational support for clinical research activities in collaboration with clinical development and clinical operations, while maintaining appropriate role boundaries
• Study Management: Manage all aspects of long-term and multi-center research projects, including Post-Marketing Studies (PMS), Investigator-Initiated Studies (IIS), and Observational Studies (OS).
• Clinical Operations: Oversights outsourced CRO (Contract Research Organization) teams to ensure projects are completed within allotted timelines and budgets in accordance with relevant SOPs.
• Data & Publication: Responsible for data collection, analysis, and interpretation, including co-authoring scientific papers for publication with investigators.

4. Medical Governance & Compliance
• Material Review: Review and approve promotional and non-promotional materials (promotional, scientific, and training) to ensure balance, integrity, and regulatory compliance.
• Medical Information: Respond to unsolicited off-label or complex medical information queries in accordance with regional and local SOPs.
• Quality Assurance: Manage and update Standard Operating Procedures (SOPs) and ensure medical approval of all studies and essential documents like protocols. 
• Protect confidential, personal, and proprietary information in accordance with applicable data protection requirements.

[QUALIFICATIONS]
1. Education: 
• University degree or higher in a relevant field of science, such as Pharmacy, Nursing, Biology, or Epidemiology.

2. Experience Requirements:
• 3+ years of experience  in Medical Affairs, including roles as an MSL, Medical Information specialist, or Study/Project Manager
• Experience working in a global or matrixed organization is highly preferred.

3. Skills & Competencies:
• Scientific Knowledge: Comprehensive knowledge of the clinical development process and relevant regulations, including GCP and local laws.
• Communication: Native in Korean and fluent in English, with strong negotiation and presentation skills.
• Technical Proficiency: Advanced skills in MS Office (Excel, PowerPoint, Word) and project management software.
• Interpersonal Skills: Proactive, strategic networking abilities, and a collaborative "Team Player" mindset.