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    更新于 1月7日

    輝瑞制藥-(高級(jí))區(qū)域醫(yī)學(xué)顧問-肺癌-上海

    面議
    • 上海靜安區(qū)
    • 1-3年
    • 碩士
    • 全職
    • 招1人

    職位描述

    藥企

    In order to maximize the value of Pfizer products to Chinese patients and heath care professional within Pfizer’s vision and mission, MSL is responsible for developing China regional medical development and life-cycle management strategy for inline products within Pfizer China business objectives and strategy independently. Establish regional platform and channel with China regional academic organization in defined therapeutic area to delivery Pfizer products message to key influencers and stakeholders independently. Build effective regional medical advisor interface and provide professional medical training to support sales teams to achieve their objectives independently.

    Develop sale team medical capability through field based medical to medical communication and KOL management independently

    • Lead mapping/ profiling of regional level KOLs.
    • Establish good academic relationship with regional academic organization at defined therapeutic area.
    • Organize and lead regional level medical to medical meeting with KOLs to deliver medical information of defined therapeutic area and assigned products
    • Cooperate with local regional medical societies to conduct medical programs/conference to facilitate new concept and state of art medical progress’ introduction to China
    • Communicate technical information, and product update to health care professionals as aligned with Pfizer China's corporate goals and objectives.
    • Collaborate with Pfizer colleagues to actively support medical and scientific meetings by medical input and insights.
    • Speak at medical communication meeting at national and regional level.
    • Meet customer medical needs and expectations with regards to assigned Brand(s) for delivery of product messages to key influencers (KOLs)

    Drive regional business decision making independently

    • Develop regional medical strategy for inline product life cycle management
    • Initiate and lead medical programs independently at regional level with internal and external customers to assist deliver product strategy and key information.
    • Collect, analyze and report timely local customer medical insights to input on product strategy and message development.
    • Work with (senior) medical advisor, product manager, regional promotion manager and sales manager proactively to assist product strategy implementation.

    Develop sale team medical capability through internal medical training independently

    • Initiate and implement independently medical activities to strengthen sale colleagues’ product and therapeutic areas knowledge at regional level.
    • Lead new sale colleagues’ medical training
    • Provide customized response for common medical queries in the field for assigned products.
    • Present at POA and regional sales meetings for medical information.

    Enhance local data generation from medical aspect to maximize products’ value and long term development

    • Discuss research concept with interested researcher, and communicated the nature and requirement of Pfizer’s IIR based on IIR strategies
    • Facilitate submission of investigator initiated pre-clinical and clinical proposals, and act as a Liaison between Pfizer and IIR researcher
    • Review and track IIR independently with good quality and required timeline
    • Facilitate research proposal screening and study placement, and follow up activities
    • Support Pfizer sponsored Non interventional study and other medical programs if applicable

    Provide medical expert opinion in safety events management to avoid negative impact.

    • Provide professional medical consultation to Safety Officer to solve Pfizer products’ safety query
    • If take clinician role: provide the clinical safety oversight including performing and documenting regular review of individual subject safety data and performing review of cumulative safety data with the safety risk lead (as delegated by the clinical lead).
    • If take clinical lead role: consistent with Safety Review Plan (SRP), performs and documents regular review of individual subject safety data, and performs review of cumulative safety data with the safety risk lead. As appropriate, the clinical lead may delegate these responsibilities to the study clinician identified in the SRP. The specific components of safety data review are detailed in the Safety Data Review Guide –for Clinicians and in SAF09 SOP. For all studies, clinical safety review should be performed in consultation with a designated medical monitor if neither clinical lead nor clinicians are medically qualified.

    Ensure company’s compliance.

    • Support Company FCPA activities: act as the sole reviewer to ensure educational grants within medical compliance as needed
    • Ensure all promotional materials are medically accurate and compliant with external and internal requirements as needed

    Partner with legal and regulatory colleagues to ensure high quality medical content of all promotional activities as needed

    REQUIRED SKILL SET

    Technical

    • Therapeutic area knowledge: familiar with the disease knowledge and clinical practice of the therapeutic area?
    • Language: Proficiency in oral and written English ?
    • Good understanding about pharmaceutical business ?
    • Computer: Good at Microsoft Office software?
    • Strong business acumen ?
    • Cross functional leadership skill?
    • Strong communication and influencing skill

    Managerial

    • Sustain focus on performance
    • Manage change
    • Seeks opportunities to receive and provide knowledge and leading practices
    • Align across Pfizer

    Certifications

    Education

    • Master degree major in clinical medicine, Master above in the defined therapeutic area is preferred

    Experience

    • Good medical knowledge for the defined therapeutic area
    • Good understanding about pharmaceutical business
    • Proficiency in English and good computer usage


    Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

    Medical

    #LI-PFE

    工作地點(diǎn)

    中信泰富廣場(chǎng)

    職位發(fā)布者

    劉一飛/RODA

    剛剛活躍
    立即溝通
    公司Logo輝瑞制藥有限公司
    輝瑞公司(Pfizer Inc.)創(chuàng)建于1849年,總部位于美國(guó)紐約,是一家以科學(xué)為基礎(chǔ)的、創(chuàng)新的、以患者為先的生物制藥公司。輝瑞的使命是“為患者帶來(lái)改變其生活的突破創(chuàng)新”。在輝瑞,我們通過科學(xué)和全球資源為人們提供治療方案,以延長(zhǎng)其生命,顯著改善其生活。在醫(yī)療衛(wèi)生產(chǎn)品的探索、研發(fā)和生產(chǎn)過程中,輝瑞始終致力于奉行嚴(yán)格的質(zhì)量、安全和價(jià)值標(biāo)準(zhǔn)。我們?cè)谌虻漠a(chǎn)品組合包括創(chuàng)新藥品和疫苗。每天,輝瑞在發(fā)達(dá)和新興市場(chǎng)的員工都在推進(jìn)人類健康,推動(dòng)疾病的預(yù)防、治療和治愈,以應(yīng)對(duì)挑戰(zhàn)我們這個(gè)時(shí)代的頑疾。輝瑞還與醫(yī)療衛(wèi)生服務(wù)方、政府和社區(qū)合作,支持并促進(jìn)世界各地的人們能夠獲得更為可靠和可承付的醫(yī)療衛(wèi)生服務(wù)。這與輝瑞作為一家全球卓越的創(chuàng)新生物制藥公司的責(zé)任是一致的。170余年來(lái),輝瑞一直致力于為所有依賴我們的人帶來(lái)改變。輝瑞于1989年進(jìn)入中國(guó)市場(chǎng)。扎根中國(guó)30余年,輝瑞已成為在華主要的外資制藥公司之一。2021年是輝瑞新征程的開始。迄今已有170余年歷史的輝瑞正在邁入全新時(shí)代,成為一家以科學(xué)為基礎(chǔ)的、創(chuàng)新的、以患者為先的生物制藥公司。目前輝瑞在中國(guó)業(yè)務(wù)覆蓋全國(guó)300余個(gè)城市,累計(jì)投資超過15億美元,并設(shè)立了1家先進(jìn)的生產(chǎn)設(shè)施,2個(gè)研發(fā)中心(分別位于上海張江高科技園區(qū)和武漢光谷),在華有近7,000名員工分布于業(yè)務(wù)、研發(fā)和生產(chǎn)等領(lǐng)域。輝瑞在華上市了五大領(lǐng)域的高品質(zhì)創(chuàng)新產(chǎn)品,包括腫瘤、疫苗、抗感染、炎癥與免疫、罕見病等多個(gè)領(lǐng)域的處方藥和疫苗,強(qiáng)大完善的產(chǎn)品線旨在滿足生命各階段的健康需求。
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