Job Description

You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise.

[Evergreen] Medical Scientific Affairs Supervisor(MSA)
Company:  B. BRAUN KOREA CO. LTD.
Job Posting Location:  Gangnam-gu, Seoul Teugbyeolsi, Korea
Functional Area:  Clinical/medical area
Working Model:  Hybrid
Requisition ID:  7507

Are you a Medical Scientific Affairs Supervisor passionate about leading and oversighting for clinical operations within Korea and supporting both company-sponsored trials (SIT) and investigator-initiated trials (IIT).? If so, this opportunity could be for you! Join us at B. Braun Korea, a leader in the medical devices industry, where your skills and experience will be recognized and celebrated. Take the next step in your career with us and help shape the future of healthcare!  
As a Medical Scientific Affairs Specialist at B. Braun you will play a vital role in….

 

Your key responsibilities:
This position is to provide leadership and oversight for clinical operations within Korea, supporting both company-sponsored trials (SIT) and investigator-initiated trials (IIT). This role is responsible for supervising junior team members, managing study execution, ensuring regulatory and operational compliance, and acting as a liaison between local office and regional/global clinical team.


Clinical Study Leadership and Oversight

  1. Lead the execution of all clinical studies (IIT and SIT), ensuring they are delivered on time, within scope, and in compliance with applicable regulations - KPI
  2. Provide strategic oversight to ensure study execution aligns with the research plan. Proactively support and actively contribute to final reports and publications in collaboration with investigators.•    Lead and ensure full compliance of study operations and documentation with internal and external guidelines/regulations, maintaining the highest standards of integrity and oversight
  3. Protocol Evaluation and Financial Stewardship
  4. Assess and validate investigator-initiated study proposals, aligning with internal stakeholders on study design and budgets, and coordinating contract readiness with relevant functions to facilitate global approval.
  5. Oversee clinical budget estimation and ensure accurate study cost payments per contract, optimizing financial efficiency and compliance - KPI
  6. Site Management and Regulatory Compliance
  7. Establish and maintain strong site and investigator relationships, enabling high-quality site performance and protocol compliance
  8. Ensure accurate and timely coordination of regulatory and HQ reports, maintaining compliance and precision
  9. Oversee timely and compliant reporting of safety events and product complaints, ensuring alignment with SOPs and corporate standards
  10. Publication Implementation, Knowledge Utilization & Strategic Engagement
  11. Support medical-scientific knowledge dissemination by contributing to clinical reports, publications, and internal sharing of results and cross-functional application - KPI
  12. Lead engagement in scientific meetings, fostering strategic relationships with technical experts, opinion leaders, and professional societies to enhance professional capabilities, optimize study implementation, and strengthen the organization's reputation
  13. Team Development and Mentorship
  14. Coach, supervise, and empower junior team members through structured training, clear expectations, and constructive feedback - KPI

What you will bring to the team: 

  • Minimum 10 years of experience in healthcare, CRO, hospital, or public organization
  • Multinational company experiences preferred
  • Proven ability to lead clinical projects, manage budgets, and oversee stakeholder negotiations
  • Strong leadership and strategic thinking, ensuring study success and operational efficiency
  • Commanding communication & stakeholder influence  
  • Decisive problem-solving & strategic decision-making  
  • Expert project governance & resource optimization  


What sets B. Braun apart?
B. Braun Korea is a leader in medical technology and healthcare solutions, established in 1990 and headquartered in Seoul. We are dedicated to enhancing patient care through innovation and excellence, offering products and systems for anaesthesia, intensive care, cardiology, extracorporeal blood treatment and surgeries.  B. Braun embraces continuous improvement and innovation and is driven by a corporate philosophy of ‘Sharing Expertise’.  We foster a culture of trust and collaboration, ensuring compliance with the highest ethical standards. This is an excellent opportunity to gain hands-on experience, contribute to impactful projects in the healthcare industry and join our shared vision – to protect and improve the health of people around the world. 

Benefits

  1. Healthcare 산업군 내에 경쟁력 있는 Benefit 제공
  2. 선택적 근무 제도, 조기 퇴근제 및 재택 근무제 운영영
  3. Flexible Benefit 수당 (복지카드 제공)
  4. 통신비 지원
  5. 생일 상품권 제공
  6. 건강검진 제공
  7. 경조사금 및 휴가
  8. 자녀학자금 (고등학교, 대학교)
  9. 장기근무 포상