Tasks
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
About Cardiovascular
At Johnson & Johnson MedTech, our Cardiovascular team develops advanced technologies for heart recovery, electrophysiology, and stroke care. We build on a strong legacy of improving outcomes for patients with heart failure, cardiogenic shock, and complex cardiovascular conditions. Heart Recovery (Abiomed) is a global leader in mechanical circulatory support and minimally invasive heart pump technology, including the Impella® platform, enabling physicians to stabilize hemodynamics and support cardiac recovery.
We are searching for the best talent for Commercial Coordinator – Heart Recovery (Abiomed) based in Seoul.
Purpose
The Commercial Coordinator plays a critical role supporting both Sales and Marketing teams while leading operational and administrative excellence for the Heart Recovery business. This position ensures efficient capital equipment processes, supports business development activities, and contributes to clinical (PMS) operations aligned with regulatory and quality requirements.
You will be responsible for:
Business Operations & Commercial Support
- Develop and manage internal processes to ensure efficient business operations, including capital equipment selling and asset management
- Execute complex administrative and business coordination tasks supporting sales and marketing initiatives
- Track and manage purchase orders, product samples, and demo equipment
- Maintain and manage business data via spreadsheets and online tools
- Support development of sales tools, programs, and internal resources
- Provide logistical and administrative support for congresses, symposiums, workshops, and internal/external events
- Communicate and coordinate with dealers and external partners to support business continuity
- Provide cross-functional support to local and regional teams as needed
PMS (Post-Market Surveillance) Operations
- Support clinical research activities to ensure safety, efficacy, and regulatory compliance of products
- Build relationships with investigators, site staff, and external vendors
- Prepare and manage clinical trial documentation (e.g., agreements, regulatory submissions, ethics dossiers)
- Perform site feasibility, initiation, monitoring, and close-out activities in collaboration with clinical teams
- Track patient enrollment, visit schedules, and protocol adherence
- Maintain data quality through CRF review and query management
- Ensure timely adverse event reporting and compliance with safety regulations
- Maintain Trial Master File (TMF) and ensure data/document integrity
- Manage clinical supplies, shipment, and inventory tracking
- Support audit readiness and respond to inspection findings
- Assist with internal/external stakeholder meetings and clinical research initiatives
Qualifications / Requirements:
- Bachelor’s degree or higher required
- At least 1 year of experience in business operations or sales administration
- Prior experience in independent clinical operations (e.g., CRA or CRC) is a plus
- Experience in the medical device or pharmaceutical industry is preferred
- Proficiency in written business English
- Strong verbal and written communication skills in both Korean
- Proficiency in Microsoft Office (Excel, PowerPoint, PDF, etc.)
- Strong organizational and multitasking skills with attention to detail
Legal Entity
MedTech
Job Type
Fixed Term (1-year contract)
Application Documents
Free-form resume AND cover letter is required (in Korean or English).
Application Deadline
Until the position is filled
Notes
- Preference will be given to individuals subject to national veterans’ benefits and persons with disabilities upon submission of relevant documents as per applicable laws.
- Only candidates who pass the resume screening will be notified individually. However, notifications may be delayed due to company circumstances.
- If any false information is found in the application documents, the hiring may be canceled even after the offer is confirmed, and future applications may be restricted.
- Submitted documents will not be returned and will be deleted upon request.
Equal Employment Opportunity
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by law.
Requirements
See above.
Information
Apply
The Others
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제출하신 서류는 일체 반환하지 않습니다.
입사지원서 내용에 허위사실이 판명될 경우 입사가 취소될 수 있습니다.
기타 문의사항은 E-mail로 문의바랍니다.
Company
Johnson & Johnson is the world's most comprehensive and broadly based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in pharmaceutical, and medical devices and diagnostics markets and have the skills and resources to tackle the world's most pressing health issues.
Want to learn more about our Operating Companies?
Consumer http://www.youtube.com/watch?v=DCI7ItXYGos
Medical Devices http://www.youtube.com/watch?v=pjisNOe2oKI
Pharmacetical http://www.youtube.com/watch?v=clj_NIWV4UE
- 영업·마케팅 운영 지원 및 내부 프로세스 관리
- 자본 장비 판매 및 자산 관리 지원
- 구매 주문, 제품 샘플, 데모 장비 추적 및 관리
- 스프레드시트 및 온라인 도구 기반 사업 데이터 관리
- 세일즈 툴, 프로그램, 내부 자료 개발 지원
- 학회, 심포지엄, 워크숍 및 내외부 행사 운영 지원
- 딜러 및 외부 파트너와의 커뮤니케이션 및 협업
- 임상 연구 운영 및 PMS 관련 업무 지원
- 임상 문서, 규제 제출 자료, 윤리 심의 자료 준비 및 관리
- 사이트 타당성 평가, 개시, 모니터링, 종료 활동 지원
- 환자 등록, 방문 일정, 프로토콜 준수 및 데이터 품질 관리
- 이상사례 보고, TMF 관리, 임상 물품 및 재고 추적
- ✓학사 학위 이상
- ✓사업 운영 또는 영업 지원 경력 1년 이상
- ✓독립적 임상 운영 경험
- ✓비즈니스 영어 문서 작성 능력
- ✓한국어 구두·문서 커뮤니케이션 능력
- ✓Microsoft Office 활용 능력
- ✓우수한 조직력 및 멀티태스킹 능력
- ★의료기기 또는 제약 산업 경험
- ★CRA 또는 CRC 경력
- ★국가유공자 및 장애인 관련 서류 제출 대상
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본 정보는 피플앤잡의 동의 및 허락 없이는 재배포 할 수 없습니다.



