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J&J Family of Companies [Janssen] Therapeutic Area (TA) Lead – ST3 (Solid Tumor Targeted Therapy) in Yongsan-gu, South Korea

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 consumer, pharmaceutical, and medical devices and diagnostics markets and have the skills and resources to tackle the world's most pressing health issues. 1. 포지션 : Therapeutic Area (TA) Lead – ST3 (Solid Tumor Targeted Therapy) 2. 계열사 : 한국얀센 (Janssen

  1. 근무지 : 서울시 용산구

  2. 근무 형태 : Regular


  • Lead the development and implementation of the medical strategy and plan of the assigned therapeutic area, including integrated evidence generation plan (IEGP) and TA IVT strategy, via close collaboration with internal/external stakeholders and alignment with the global/regional TA medical strategy as well as TA business strategy. and Review medical/ promotional materials within assigned therapeutic areas [Medical Advisor/Therapeutic Area Lead]

  • Be responsible to review study proposals and reports/manuscripts from Company sponsored studies to investigator-initiated studies [Study Responsible Physician/Scientist]

  • Define MSL/Medical strategy aligned with brand strategy based on generated medical insights and Lead MSLs to ensure full implementation of medical plans by coaching and supporting [MSL/Medical Advisor Manager]

  • Solid Tumor Medical Advisor, Lung Cancer MSL and Prostate Cancer MSL are reporting to Solid Tumor TA Lead.


  • Act as a Medical Affairs Expert and lead the development and implementation of the medical strategy for a specific product (group of products) or franchises

  • Provide expert medical leadership for other internal functions (Medical, Commercial, Regulatory affairs, Market Access etc.)

  • Lead integrated evidence generation plan (IEGP) process with TA cross function teams

  • Build up or enhance a trusted collaboration with the external scientific community in order to facilitate a continuous communication and transfer of knowledge, from key opinion leaders and a wider group of physicians and customers

  • For Medical Education activities, support the MSL/Medical Advisor on Medical Education programs concept, review the program proposals and final program outline and support the review of scientific Medical Education materials

  • Review promotional materials with ensuring brand messages relating to allocated products

  • Work with AP teams to gather local inputs and to drive alignment of strategy/plan for the assigned product plans for designated TAs

  • Support Medical Affairs to evaluate proposals of IISs for scientific soundness and whether those are in alignment with the medical strategy

  • Provide local country feasibilities for global R&D programs, such as epidemiology, current clinical practice, on-going competitor studies etc. upon a request of GCO

  • Recommend relevant investigator sites considering available patient pools, site capabilities and future company business plans

  • Define MSL and Medical Advisor strategy within Medical Affairs and Lead MSLs/MA to ensure full implementation of the Medical Plans

  • Strengthen external customer management in the field by building up the capability and capacity of MSLs to ensure high quality scientific engagement

  • Recruit and establish a qualified MSL team

  • Inspire and motivate them by active, open and constructive communication

  • Support the Country Medical Director in the execution and supervision of all country Medical activities

  • Ensure safety reporting requirements (timely AE/PQC reporting) as set out in company policies and SOP’s (Standard Operating Procedures) are met and appropriately managed when planning projects, developing materials, executing projects and contracting vendors

  • Ensure relevant quality, medical, HCC and legal compliance requirements are fully understood, appropriately managed and complied with when planning projects, developing materials, executing projects and contracting vendors

  • Proven leadership in people management and development regardless of direct authority, embracing diversity, equity and inclusion


  • At least 3 years’ experience in medical affairs in pharmaceutical industry is strongly preferred

  • Understanding of local regulatory policy and industry’s code of practice related to drug registration, pharmaceutical promotion, and clinical study

  • In-depth scientific and/or therapeutic knowledge, strength in research and interpretation of scientific publications

  • Knowledge for research, clinical trial design and process, national healthcare and access system

  • Interpersonal and communication skills to effectively interact with a broad range of external and internal personnel

  • Excellent English language skills, spoken and written

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Primary Location

South Korea-Seoul-Yongsan-gu-


Janssen Korea, Ltd. (7220)

Job Function


Requisition ID