TIFFANY & CO.
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[Sinclair] Medical Affairs Manager, APAC

서울 강남 / 잠실 의사,약사,간호사 2026.09.02 ~ 채용시

Tasks

Sinclair is Hiring! Join Our Team as a Medical Affairs Manager, APAC 🚀
We are currently recruiting for Medical Affairs Manager for APAC in South Korea, HK and Singapore.

About Sinclair
Founded in 1971, Sinclair is a global medical aesthetics organisation, that delivers an extensive product range. With an in-house commercial infrastructure, including manufacturing and a network of distributors in leading global markets, our products are sold in 55 countries worldwide.
This is a great time to join Sinclair as we continue to increase our product range and expand into new markets and territories.

Sinclair Values:
✅ Act with Integrity Consistently doing the right thing even when it’s the hard choice; 100% Compliance with all rules, standard operating procedures and guidelines✅ Results-Driven Make a business impact in all you do, whether sales, efficiency, operational excellence; it should make a meaningful impact✅ Innovation-Centered Redefining Aesthetics, we must be pioneering in how we do business; this can be in products, in service models, or strategy✅ One Company, One Goal Working towards unified mission, we are all Sinclair and be seen by customers as one company in every way
✅ Own It! Be Accountable for your decisions, actions and consequences; Be Reliable to your customers and colleagues

What You'll Be Doing:
🔹 Lead and coordinate clinical trial projects; ensure all local clinical trials are delivered on schedule and within budget, in strict compliance with ICH GCP, NMPA guidelines, and company policies. Collaborate with RA to develop clinical trial protocols supporting regulatory strategy and new product registrations.
🔹 Ensure the local pharmacovigilance function operates efficiently and in compliance with local regulations and company/partner policies. Serve as Local Safety Officer, covering medical assessment, training, adverse event reporting, device deficiency reporting, and trend analysis across both pharmaceutical and medical device portfolios.
🔹Conduct internal medical training programs on company products. Provide regularly updated publications and training materials to enhance scientific knowledge and acumen across the organization.
🔹Review and approve local promotional materials in compliance with local regulations and company standards.
🔹Serve as the medical contact for local KOLs and external experts. Convene advisory boards and KOL meetings across key therapeutic and aesthetic areas to gather treatment insights and real-world clinical experience.
🔹Provide in-depth medical evaluation for strategic licensing and business development partnerships.
🔹Partner with regional and national organizations to develop effective patient medical education and engagement programs.
🔹Oversee clinical evidence generation for aesthetic medical devices, including PMCF studies and real-world evidence collection to support product claims and lifecycle management. Lead medical input for treatment protocols and HCP clinical training.
🔹Monitor the competitive clinical landscape in the aesthetic/medical device space and provide medical strategy recommendations to commercial and marketing teams.
🔹Build and maintain a high-quality, high-performing Medical Affairs and PV team, and foster talent development.



Perks & Benefits:
💰 Competitive Salary & Performance Bonuses📈 Career Growth & Learning Opportunities🏥 Health & Wellness Benefits🎉 Fun Team Events & Supportive Culture

We have a real focus on developing our people, and by fostering an entrepreneurial culture, we encourage flexibility, accountability and autonomy. The company is full of opportunity for those who wish to grasp it. Our people thrive on engagement, development and a varied workload. You will often be included in projects that require you to collaborate cross-functionally.
This is an exciting opportunity to join a successful company, with big ambitions for the future.
If this sounds like you and you meet the requirements, please apply, we would love to hear from you.
Please note if we receive a high volume of applications, we may close the role before the closing date noted.
By making this application you give consent for personal information to be used in automated decision-making processes relating to key job requirements which are stated in this ad.

Sinclair does not accept speculative or unsolicited CVs from Recruitment Agencies. Any unsolicited CVs received will be treated as property of Sinclair and Terms & Conditions associated with the use of such CVs will be considered null and void

Requirements

Your skills and experience
Essential:
🔹Medical degree or Ph.D., or equivalent doctoral-level degree in a relevant scientific or medical field.
🔹Fluent in English (written & spoken)
🔹Experience supporting injectable aesthetics, biostimulators, dermal fillers, energy-based devices, or other aesthetic medical devices is highly desirable.
🔹Strong problem solving and root cause analysis capability
🔹Experience managing or overseeing a company pharmacovigilance function.

Desirable:
🔹Experience in interacting with NMPA/CDE
🔹Specialization or clinical experience in Dermatology, Plastic Surgery, or Aesthetic Medicine
🔹Outstanding cross functional influencing, facilitation and conflict resolution skills; able to drive alignment without direct authority.
🔹Ability to operate in fast paced, multi-cultural global environment, manage multiple competing priorities.

Information

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Company

외국계기업 제약바이오
서울시 송파구 올림픽로35다길 13, 국민연금공단 송파지사 7층 (우)05510

한국싱클레어는 피부미용성형시장의 아시아 No.1을 목표로 미용성형관련 의료기기 및 Cosmeceuticals를 수입,제조하는 회사입니다.
현재 폐사는 원제조사인 `싱클레어(Sinclair)`사의 한국지사 입니다.
따라서 최종입사자는 입사와 동시 본사의 마케팅 교육 연수의 기회가 주어질 것입니다.
싱클레어사는 에스테틱, 운드케어, 스킨케어 전문의 영국계 글로벌 기업으로서 지속적인 연구개발과 투자로 최고의 피부미용성형 전문기업을 목표로 하고 있습니다.


직무 Medical Affairs Manager
🛠 관련 기술 ICH GCP NMPA CDE PMCF
핵심 업무
  • 임상시험 프로젝트 총괄 및 조율
  • 지역 임상시험 일정·예산 관리 및 ICH GCP, NMPA, 사내 정책 준수
  • RA 협업을 통한 임상시험 프로토콜 개발 및 인허가 전략 지원
  • 지역 약물감시 기능 운영 및 규정 준수 관리
  • Local Safety Officer 역할 수행 및 이상사례·기기 결함 보고, 추세 분석
  • 사내 의료 교육 프로그램 운영 및 과학 자료·교육 자료 업데이트
  • 지역 홍보물 의학적 검토 및 승인
  • KOL 및 외부 전문가 대응, 자문회의 및 KOL 미팅 운영
  • 전략적 라이선싱 및 사업개발 파트너십 의학적 평가
  • 환자 의료 교육 및 참여 프로그램 개발 협업
  • PMCF 연구 및 실사용근거 수집을 통한 임상 근거 생성 관리
  • 치료 프로토콜 및 HCP 임상 교육에 대한 의학적 지원
  • 경쟁 임상 환경 모니터링 및 의료 전략 제안
  • Medical Affairs 및 PV 팀 구축·육성
필수 요건
  • 의학 학위 또는 관련 과학·의학 분야 박사 학위
  • 영어 구사 능력
  • 주사형 에스테틱, 바이오스티뮬레이터, 더말 필러, 에너지 기반 장비 등 에스테틱 의료기기 관련 경험
  • 문제 해결 및 근본 원인 분석 능력
  • 회사 약물감시 기능 관리 또는 감독 경험
우대 요건
  • NMPA/CDE 대응 경험
  • 피부과, 성형외과 또는 에스테틱 의학 전공 또는 임상 경험
  • 우수한 부서 간 영향력 발휘, 조율 및 갈등 해결 능력
  • 빠른 속도의 다문화 글로벌 환경에서의 복수 우선순위 관리 능력
BETAAI가 공고 원문에서 추출한 참고 정보입니다.
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