• 求人番号：Job-00223607 掲載日：2023-01-28

  MSL Cardiovascular

  MSL

  700 - 1000 万円 東京 製薬 看護師

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  会社概要

  本格的な研究・開発で医療に本質的に貢献できる医薬品の開発に力を注いでいる製薬会社です。

  業務内容

  1 To build activity plan based on IBP / ICP / ICE To identify EE in the responsible therapeutic area and revise. list accordingly ・ To develop appropriate EE engagement plan based on IBP / TA strategy in the responsible therapeutic area 
  
  2 EE engagement consistent with IBP / ICP / ICE Execution of plan and its record To record and excute EE engagement plan aligned with IBP / ICP / ICE Implement SI / Scientific exchange to obtain scientific insights on the products in charge from EE. Also, create appropriate content for that purpose. In addition, Scientific Insights, including the latest information from academic societies, will be shared with related departments to formulate strategies and action plans. To conduct SI / Scientific Exchange in order to gain scientific insight on responsible product from EE And to create appropriate contents. Also, to share scientific insight including latest information from congress, etc. with relevant departments to develop strategies and action plans ・ Support the organization of advisory boards that plan and implement in the area of ​​disease in charge, and plan and implement scientific meetings. To support planning and organization of advisory board for execution in the responsible therapeutic area as well as planning and implementation of scientific meetings ・ Regular contact / communication with the target EE to build and maintain good relationships throughout the product life cycle. To build and sustain positive relations with target EE throughout product life cycle via regular contact and communication ・ Use digital tools to build relationships with customers. To utilize digital tools in customer engagement ・ Record and manage budget for all activities. To manage budget and leave record for responsible activities as a whole 
  
  3 To provide support for IIS and data building To create new scientific data that considers feasibility, scientific appropriateness, and ethics to fill data gaps and unmet needs. new scientific data in consideration of feasibility, scientific appropriateness and ethics in order to fill data gap and unmet needs ・ Support clinical / non-clinical IIS as liaison based on reques 
  
  4 To provide scientific data on approved / unapproved / off-label products based on customer's request. Create appropriate content according to EE and other scientific questions and requests from medical personnel, and provide appropriate information after obtaining approval within the area of ​​the disease in charge. To create appropriate contents based on request and scientiic question from EE and other medical personnel as well as to provide appropriate information on top of full approval within responsible therapeutic area To attend speaker trainings to conduct scientific contents training and to answer questions based on request
  
  5. MR training MR Training In order to improve the knowledge level of MR, in response to requests from the training department, To conduct MR training in order to improve knowledge level of MR, based on request from training department
  
  6. To comply with Code of Conduct / Laws and RegulationsUnderstand and comply with laws and regulations, industry rules (promotion code, fair competition rules, personal information, data collection / storage, etc.) and related SOPs. To understand and comply with regulations and industry rules (promotional codes, fair competition rules, privacy, data collection / storage, etc.) as well as related SOP
  Be aware of employees and act in accordance with social norms and internal code of conduct. .. To act according to social norms and company's code of conduct with full awareness as a responsible employee
  

  

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