MA醫學顧問
職位描述
Responsible for providing specialist/expert advice a single area of Medical affairs - eg Compliance, medical excellence, pharmaco-economics. May also be a more unique role responsible for multiple areas of medical affairs. Role holder will be deemed an expert in their field, and will be expected to influence on a strategic level. May also manage other Medical affairs specialists.Job Description?JOB PURPOSE 工 作 目 的?An external and internal facing role that provides medical and clinical expertise in priority therapeutic areas and builds AZ scientific leadership. Medical advisor is responsible to medical plan preparation. In addition, the Medical Advisor will input into Brand Strategy and LCM and take the lead in the design and implementation of medical activities aligned with Brand Strategy. The role focuses on the development of professional relationships with KEE, building deep scientific understanding of AstraZeneca compounds by engaging KEE in study, scientific exchange meetings and advisory board meetings. Further internal accountabilities include the delivery of medical education and clinical support to medical professionals, training sales teams and involvement in development of brand strategy.?There are 4 levels in medical advisor role, i.e. associate medical advisor, medical advisor, Sr. medical advisor and principal medical advisor.?Medical advisors are expected to have ≥1 year’s experience as associate medical advisor and proven record of success (internally or externally). Sr. medical advisors are expected to have ≥2 years’ experience as medical advisor and proven record of success (internally and externally). Principal medical advisors are expected to have ≥2 years’ experience as Sr. medical advisor, basic coaching skill and proven record of success (internally or externally).? DUTIES & RESPONSIBILITES / 主 要 職 責?To establish AstraZeneca as a scientific leader through proactive, updated and effective Medical input?Develop and implement the local medical plan to address unmet medical needs in priority disease areas and ensure alignment with the brand plan.?Provide medical input for the development of company’s Brand plans?Provide the AZ internal stakeholders with an understanding of the local medical community, clinical practice, trends and real or perceived gaps in current scientific knowledge and medical treatment, competitive intelligence?Develop and implement pre-launch medical plan/activities for new products at least 2 years prior to the planned launch in the country to address key clinical and scientific challenges?Provide medical leadership on faculty and content development for medical programmes including national congresses, advisory boards, scientific exchange meetings, publications, CMEs to meet identified needs?Provide medical input to global protocols, study feasibility and local customer’s research initiatives.?Feedback from participants?Feedback from business partners on quality of contribution to Medical and Brand plans –collected by line manager?Feedback on congress report/highlights shared with cross-functional team as planned – completed feedback templates??Provide medical input into the Life Cycle Management of priority brands and TAs to meet unmet medical needs?Participate as key member of brand team as strategic partner towards LCM actions?Develop NIS or registry studies to address unmet medical needs?Initiate discussions with customers to develop studies that will fulfill global and local business strategies.?ESR Proposals- Number?For NIS number of sites, KEEs, investigators involved in studies versus plan?Timely publications of studies completed??Governance and ensuring overall adherence to processes and regulation?Provide medical input to the creation, development and agreement of promotional material and ensure all material is in line with internal SOPs and meets IFPMA code?Support Clinical team to select appropriate investigators and sites optimising quality, delivery and commercial benefit?Ensures compliance with AZ code of conduct, Corporate Governance, Audits requirement, guidelines, codes, policies and procedures?Ensures that company confidentiality is maintained (i.e. intellectual property, product, strategic and salary information)?Discloses potential breach of codes or conducts??External Medical & Scientific engagement?Build, enhance and maintain the engagement with key external expertise (KEE).?Proactively identify HCPs with high levels of scientific expertise in local treatment practice to collaborate on specific medical marketing activities?Development and implementation of KEE engagement plan in collaboration with line manager.?Develop database of KEEs and also provide recommendations for advisory board participation, potential speakers and train speakers as appropriate.?Develop own scientific knowledge and share emerging data with HCPs, discussing all aspects of the data in a scientific, objective and balanced way. Disseminate results of studies completed to medical community by translating their clinical values and incorporating into business strategies.?Respond to unsolicited requests for information about unapproved AZ products or unapproved uses of approved products, presenting such information in an objective, scientifically balanced, substantiated manner.??Develop or initiate scientific programs to explore unmet medical needs in priority disease area(s)?Discuss potential involvement in ESR and RWEs. Interact in the field with KEEs for clinical trials, ESRs?Able to conduct discussions on clinical trials in terms of study design and feasibility??Continuously demonstrate development of scientific expertise in disease area(s) of company focus?Positive engagement and response to coaching and feedback received from line manager.?In daily work takes time to reflect on customer interactions and works on areas agreed with line manager as priorities for development.?Develop behaviours to enhanced effectiveness as outlined in Competency definitions.?Proactively demonstrate the AZ Values?Active participation in AZ training, projects, and meetings depending on development needs??Compliance with relevant company and industry code of Conduct and also to comply with local country codes?Keep regular update and operate within the relevant Codes of Conduct, Ethical Interactions (EI), including GPEI and SOPs?Be sure to understand AZ policies when engage to KEEs and external stakeholders??JOB REQUIREMENTS & COMPETENCIES / 工作要求和勝任能力?Academic / Professional qualification / 學 歷 / 專 業 資 格?Master or advanced degree in clinical qualification, with 2+ year on relevant experience of medical affairs in pharmaceutical company?Bachelor degree, 2+ years doctor experience and 2+ years on relevant experience of medical affairs in pharmaceutical company??Technical / skill training / 技 術 / 技 能 訓 練?Qualified Medical Doctor?Experience of Medical Affairs function within a pharmaceutical industry?Extensive experience in relationship and stakeholder management?Project management experience?
企業簡介
阿斯利康是全球領先制藥公司,由前瑞典阿斯特拉公司和前英國捷利康公司于1999年合并而成。阿斯利康在6大治療領域為患者提供富于創新,卓有成效的醫藥產品,包括消化、心血管、腫瘤、中樞神經、麻醉和呼吸等,其中許多產品居于世界領先地位。
阿斯利康總部位于英國倫敦,研發總部位于瑞典。產品銷售覆蓋全球100多個國家和地區。2005年公司銷售收入為240億美元。
阿斯利康擁有強大的研發能力,平均每個工作日的研發投入達到1400萬美元 (2005年研發總投入為34億美元)。我們在7個國家設有11個研發機構,共有11,900名員工從事與新藥研發相關的工作。
阿斯利康擁有極具希望的早期開發產品組合,共有45個項目處于臨床前研究階段、17個項目處于一期臨床研究階段、13個項目處于二期臨床研究階段、6個項目處于三期臨床研究階段。
阿斯利康在全球19個國家有27個生產基地,共有14,000名員工致力于為客戶提供安全、有效、高質量的產品。
阿斯利康在全球共有65,000名員工,從事醫藥產品和醫療服務的研發、生產和銷售業務。
阿斯利康被列入道瓊斯可持續發展指數(全球)以及顯示企業良好社會責任度的富時社會責任指數(FTSE4Good Index)。
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職位發布日期: 2025-03-31