製薬勤務医師 [ID: 0021]

国内大手製薬メーカー Medical Unit Head (Medical Director), Therapeutic Area Gastroenterology or Hematology

  • 会社区別国内大手製薬メーカー
  • 職種Medical Unit Head (Medical Director), Therapeutic Area Gastroenterology or Hematology
  • 勤務地東京
  • 年収~1600万円

資格・要件

Expertise in relevant disease or therapeutic area
At least 5 years of relevant medical affairs and/or clinical affairs experience with demonstrated ability to design and execute evidence generation studies and interpret evidence/data to drive optimal patient care and Japan reimbursement.
Excellent medical engagement skills
Effective matrix leadership competency
Awareness of the healthcare environment in Japan and needs of external customers
Excellent English skills
Consideration will be given to a qualified candidate with less than 5 years of medical affairs experience, who otherwise possesses specialty or sub-specialty training, demonstrates exceptional capabilities on scientific expertise, strategic vision, currently with substantial influence on medical/scientific network and high learning agility
LICENSES/CERTIFICATIONS:

Basic:

M.D. license
Good moral standing in relevant Medical Society
Must have clinical science background in relevant disease/scientific area
Business English certification or TOEIC over 800
Preferred:

Ph.D. degree with research experience
Specialty board certification
Management skills, such as MBA, Project Management Professional (PMP), or currently studying MBA, PMP

職務内容

Lead the design product-related overall strategy of Japan Medical Affairs plan (MAP), integrating Japan environment needs and medical voice of customer (patients, providers), in collaboration with relevant internal stakeholders such as Medical Research Excellence (MRE) and GMA teams and ensure alignment with global brands
Develop medical brand narrative to ensure product value is understood and specific disease area is managed to address unmet medical need
Design study concept of required evidence generation activities to meet MAP objectives
Take initiative at defining evidence generation work needed for products discussed at the JMO Medical Matrix Team (MMT) when serving as a back-up of MF Head)) and Product Strategy Team (PST, when serving as a back-up to Medical Lead or ML).
Lead the Medical Product Launch Hub to drive alignment across the MF team, provide supervision and collaborate with cross-functional and cross-department stakeholders of the specific disease areas during launch and ensure optimization of medical launch plans and meet desired objectives
Represent JMO MF in product-related committees such as Global Project Teams (GPT) or Global Medical Strategy Teams (GMST), as well as in the pipeline/pre-launch sub-GPT committees in Japan (JDT)
Support the MF Head to analyse competitive intelligence (i.e. Healthcare environment impacting the Therapeutic Area (TA), healthcare system, competitors, regulatory requirements within and outside of Japan, clinical development plan, life cycle management, insights from Medical Engagement or other matrix teams), and incorporate those in the strategies and plans
Serve as subject-matter expert involving evaluation of proposed IISRs and the application to JMO Research & Education Grants, in collaboration with relevant internal stakeholders such as MRE team
Recommend scientifically appropriate measures for health outcomes research (planned by JPBU Reimbursement Group) over the lifecycle of the medicine(s) to meet Japan reimbursement needs.
Scientifically engage external communities throughout the product life cycle to advance scientific and medical understanding of assigned products including the appropriate development and product use, management of disease and patient care
Design TA-specific post-authorisation value dossier with internal stakeholders (i.e. MRE, Market Access and Public Affairs teams)
Partner with relevant stakeholders to ensure delivery of all assigned medical activities to support life cycle management while ensuring integrity of scientific content
Apply sound medical monitoring / governance for all MF-related medical activities
Lead the development of scientific skills of internal audience (JMO department staff and commercial functions as necessary) on the relevant product and disease expertise
Act as back-up to the Medical Scientific Information physicians to review and approve educational and sales materials for medical and scientific accuracy

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