MA医学顾问
职位描述
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 职 责•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 / 工作要求和胜任能力•Academic / Professional qualification / 学 历 / 专 业 资 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 术 / 技 能 训 练•Qualified Medical Doctor•Experience of Medical Affairs function within a pharmaceutical industry•Extensive experience in relationship and stakeholder management•Project management experience•
企业简介
阿斯利康是全球领先制药公司,由前瑞典阿斯特拉公司和前英国捷利康公司于1999年合并而成。阿斯利康在6大治疗领域为患者提供富于创新,卓有成效的医药产品,包括消化、心血管、肿瘤、中枢神经、麻醉和呼吸等,其中许多产品居于世界领先地位。
阿斯利康总部位于英国伦敦,研发总部位于瑞典。产品销售覆盖全球100多个国家和地区。2005年公司销售收入为240亿美元。
阿斯利康拥有强大的研发能力,平均每个工作日的研发投入达到1400万美元 (2005年研发总投入为34亿美元)。我们在7个国家设有11个研发机构,共有11,900名员工从事与新药研发相关的工作。
阿斯利康拥有极具希望的早期开发产品组合,共有45个项目处于临床前研究阶段、17个项目处于一期临床研究阶段、13个项目处于二期临床研究阶段、6个项目处于三期临床研究阶段。
阿斯利康在全球19个国家有27个生产基地,共有14,000名员工致力于为客户提供安全、有效、高质量的产品。
阿斯利康在全球共有65,000名员工,从事医药产品和医疗服务的研发、生产和销售业务。
阿斯利康被列入道琼斯可持续发展指数(全球)以及显示企业良好社会责任度的富时社会责任指数(FTSE4Good Index)。
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职位发布日期: 2025-03-31