At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Medical Affairs **Job Category:** Scientific/Technology **All Job Posting Locations:** Seoul, Korea, Republic of **Job Description:** **About Innovative Medicine** Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine The **Medical Advisor** will play a critical role in overseeing the medical aspects of J&J upcoming pipelines and relevant disease areas. This individual will act as a medical expert who is focusing on upcoming disease areas, collaborating with various internal stakeholders, and supporting local engagement in global pivotal trials to ensure the successful development and commercialization of products. **[Medical Advisor for upcoming Therapeutic areas]** **Medical Expertise** representing KR Medical affairs in upcoming disease areas: + Provide in-depth medical knowledge and insights on emerging disease areas relevant to the pipeline. + Serve as a subject matter expert for internal teams and external stakeholders regarding products and therapeutic areas. + Provide expert medical leadership in the Global Filing and Launch Strategy + Lead local Integrated Evidence Generation Plan discussion and participate in regional IEGP as a local medical representative **Tight Collaboration** with several functions in local/regional + Partner with cross-functional teams, including New Product Introduction (NPI), Regulatory Affairs (RA), and Medical Affairs (MA), to align strategies and objectives. + Partner with regional medical affairs and other cross-functional teams in North Asia or Asia Pacific to provide local inputs and drive alignment of strategy/plan for upcoming disease areas + Facilitate the integration of medical insights into development and commercialization plans (e.g. Integrated Value Team , GFLS meetings) + Transfer medical/practical knowledge to internal collaborators **Stakeholder Communication:** + Build-up and maintain external relationship with local academic society as well as local KIs/Investigators in order to facilitate partnership continuity and transfer knowledge + Leverage relationships with local investigators and KIs to gain inputs medical/practical inputs into developing pre-launching strategies + Act as the key point of contact for medical inquiries related to pipeline compounds and disease areas. **[Study Responsible Physician/Scientist]** **Support Global Development Programs** via tight collaboration with GCO + 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 investigators and study sites considering available patient pools, site capabilities and future company business plans + Engage with local investigators/sites for boosting enrollment, issue management etc. upon a request **Lead Investigator-Initiated Study (IIS) & Local Company-sponsored study** with RWE/MADU + Communicate with investigators from evaluating the IIS proposals in the view of scientific soundness and alignment with the company strategies + Lead in developing study ideas and study initiation under the J&J internal processes e.g. MEC, ReCAP, PRC etc + Support clinical operations via collaboration with RWE and MADU team in study start-up meetings and other activities to provide the appropriate training and information to investigators and site personnel. + Review and finalized CSRs of local studies **Lead Publications** + Support the development and implementation of the publication plan at local/regional level. + Develop manuscripts until publication **Ensure that J&J guidelines for publication are followed, and that all MAF studies are published in accordance with J&J policy.** **Continuous Learning:** + Continuous developing disease knowledge by self-driven learning + Stay up-to-date with the latest developments in research, clinical practices, and regulatory guidelines. + Foster a culture of learning and continuous improvement within the team. **Compliance** + Ensure safety reporting requirements (timely AE/PQC reporting) as set out in company policies and SOP’s (Standard Operating Procedures) + Ensure relevant quality, medical, HCC and legal compliance requirements are fully understood, appropriately managed and complied **Preferred Experiences;** + At least 1-2 years’ experience in clinical practice or at least 5 years’ experience in pharmaceutical industry is preferred + Experience in rare diseases, cardiology, or companion diagnosis is preferred + Understanding of local regulatory policy and industry’s code of practice related to drug registration, pharmaceutical promotion and clinical study. **LIST JOB SPECIFIC COMPETENCIES/SKILLS REQUIRED:** + Strength in research and interpretation of medical data + Strong agility for self-driven learning + Strong leadership, personal integrity and demonstrated customer focus + Demonstrated capabilities for a field based medical role and proven competency at the Senior level + Proven ability to lead and coach scientific/medical personnel at all skill and knowledge levels + Proven ability to interpret, communicate and implement medical/scientific strategies + Excellent interpersonal, communication, negotiation and presentation skills + Must be able to organize, prioritize, and work effectively on multifunctional teams in a constantly changing environment + Demonstrated ability to work in a cross functional environment + Understand local regulatory policy and industry’s code of practice related to drug registration, pharmaceutical promotion and clinical study + Awareness of, and adherence to, Johnson & Johnson Credo values and International Health Care Business Integrity Guide **Legal Entity** Innovative Medicine(Formerly Janssen) **Job Type** Regular **Application Documents** Free-form resume AND cover letter is preferred (in Korean or English). **Application Deadline** Open 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.