한국휴렛팩커드
월트디즈니컴퍼니코리아

Observational Research Manager

서울 바이오,의약,제약 / 의료기기 2026.11.02 ~ 2026.11.30

Tasks

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Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer.  As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

[Observational Research Manager]

What you will do

Position Summary
Join Amgen’s Center for Observational Research (CfOR) to generate high-quality real-world evidence that informs drug development, product safety, regulatory decision-making, and evidence-based healthcare.
As Observational Research Manager, you will support pharmacoepidemiology and causal inference activities across East Asia, with an initial focus on Korea and Japan.  You will contribute epidemiologic expertise to product safety, benefit-risk assessment, regulatory evidence generation, and other real-world evidence needs across the product lifecycle and help strengthen regional research capabilities.
You will serve as a strong scientific contributor to study protocols, analyses, regulatory and scientific communications, and peer-reviewed publications supporting Amgen's research and development objectives.
Reporting to the Regional Epidemiology Head of Data and Analytics Center, this position will be based in Seoul, South Korea, with flexibility for remote work within Korea, subject to company policy.  This role may require occasional travel within East Asia to support regional collaboration and deepen understanding of local healthcare systems and real-world data capabilities.
 
Key Activities:

  • Design and execute pharmacoepidemiology studies addressing product safety, benefit-risk assessment, regulatory requirements, and other priority evidence questions across the product lifecycle.
  • Apply epidemiologic and causal inference methods and use appropriate real-world data sources to address scientific questions.
  • Lead interpretation of real-world evidence on adverse events, risk factors, background rates, and treatment outcomes.
  • Collaborate across East Asia and globally with epidemiology, safety, regulatory, medical, and data science teams to define evidence and appropriate study approaches.
  • Contribute epidemiologic expertise to regulatory submissions, post-marketing requirements and commitments, risk management activities, and other product safety initiatives.
  • Develop study protocols, analysis plans, study reports, scientific presentations, and peer-reviewed publications, while contributing to external scientific understanding and appropriate use of real-world evidence methods.


Requirements

What we expect of you

Basic Qualifications

  • Doctorate degree in Epidemiology, Pharmacoepidemiology, Public Health, or related discipline with substantial observational research training
  • Experience designing, executing, analyzing, and interpreting pharmacoepidemiologic research within a pharmaceutical, biotechnology, academic, or public health setting
  • Experience planning and managing observational research projects
  • Ability to work effectively across multidisciplinary and cross-functional teams across geographies
  • Strong scientific writing, presentation, and communication skills in English

 
Preferred Qualifications

  • Experience applying causal inference methods, including target trial emulation or causal roadmaps, to generate real-world evidence.
  • Experience using secondary healthcare data, including claims, electronic medical records, registries, or other large-scale healthcare databases in East Asia
  • Korean, Japanese, or Chinese language capability.


What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.
Apply now and make a lasting impact with the Amgen team. 
careers.amgen.com


As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.
We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.

Information

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제출서류

한글이력서, 영문이력서 (각종 증빙서류는 서류전형합격자에 한해 추후제출)

접수방법
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The Others

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기타 문의사항은 E-mail로 문의바랍니다.

Company

서울특별시 중구 을지로5길 19, 20층(수하동, FERRUM TOWER) 20th Floor, Ferrum Tower, 19 Eulji-ro 5-gil, Jung-gu, Seoul

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Our Mission: To Serve Patients 

암젠은 생명과학(Biology)과 기술(Technology)의 강점을 결합하여, 인류가 직면한 어려운 질병에 맞서 사람들의 삶이 편리하고 풍요롭게 지속되도록 돕고 있습니다.
1980년 미국 캘리포니아 사우전드 오크스(Thousand Oaks)에서 설립된 암젠은 생명공학 산업의 기틀 마련에 기여했으며, 이후로도 산업 성장을 지원해 왔습니다. 암젠의 연구개발(R&D) 투자는 기존 의약품 포트폴리오를 기반으로 암질환 ∙ 심혈관계질환 ∙ 비만 및 비만 관련 질환 ∙ 염증성질환 ∙ 희귀질환 치료 분야에서 강력한 파이프라인을 구축하고 있습니다.

암젠코리아는 2015년에 출범하여 ‘환자를 위한다(To Serve Patients)’라는 사명 아래 암질환 ∙ 골질환 ∙ 심혈관질환 ∙ 희귀질환 분야에서 국내 환자들을 위한 혁신적인 의약품을 공급하고 있습니다. 또한, 암젠의 생명공학 기술을 기반으로 한국의 생명공학 산업과 사회 전반에 기여할 수 있는 다양한 활동을 전개하고 있습니다. 이러한 노력은 2024년 보건복지부 혁신형 제약기업 인증으로 이어져, 한국 사회에 대한 기여를 다시 한번 인정받았습니다.

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We helped establish the biotechnology industry, and we remain on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. Our investment in research and development has yielded a robust pipeline that builds on our existing portfolio of medicines to treat cancer, heart disease, osteoporosis, inflammatory diseases and rare diseases.

Amgen is one of 30 companies comprising the Dow Jones Industrial Average®, and part of the Nasdaq-100 Index®. In 2024, Amgen was named one of the “World’s Most Innovative Companies” by Fast Company and one of “America’s Best Large Employers” by Forbes.


직무 관찰연구 매니저
핵심 업무
  • 약물역학 및 인과추론 연구 설계·수행
  • 실사용근거 기반 제품 안전성 및 유익성-위해성 평가
  • 이상반응, 위험요인, 배경발생률, 치료결과 해석
  • 동아시아 및 글로벌 유관팀과의 연구 접근법 협업
  • 규제 제출자료, 시판 후 요구사항, 위험관리 활동 지원
  • 연구계획서, 분석계획서, 연구보고서, 학술발표, 논문 작성
필수 요건
  • ✓역학, 약물역학, 공중보건 또는 관련 분야 박사 학위
  • ✓제약, 바이오테크, 학계 또는 공중보건 분야의 약물역학 연구 설계·수행·분석·해석 경험
  • ✓관찰연구 프로젝트 기획 및 관리 경험
  • ✓다학제 및 지역 간 협업 역량
  • ✓영어 과학적 문서 작성, 발표, 커뮤니케이션 능력
우대 요건
  • ★인과추론 방법 적용 경험
  • ★Target trial emulation 또는 causal roadmaps 활용 경험
  • ★청구자료, 전자의무기록, 레지스트리 등 2차 의료데이터 활용 경험
  • ★동아시아 대규모 의료 데이터베이스 활용 경험
  • ★한국어, 일본어 또는 중국어 구사 능력
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