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更新于 4月28日

(高級)醫(yī)學(xué)顧問-廣闊市場

2-3.5萬
  • 北京東城區(qū)
  • 3-5年
  • 碩士
  • 全職
  • 招1人

雇員點(diǎn)評標(biāo)簽

  • 同事很nice
  • 團(tuán)隊(duì)執(zhí)行強(qiáng)
  • 工作環(huán)境好
  • 人際關(guān)系好
  • 氛圍活躍
  • 實(shí)力大公司

職位描述

藥企
Why Patients Need You Field-based medical colleagues provide therapeutic area /product expertise to health care providers. You will think big and demonstrate every day that we're a patient-centric company by looking to improve health outcomes for patients. What You Will Achieve To advise and manage medical related activities in all operations of company with medical expertise and company policies, with the objective of ensuring the scientific validity and the ethics of operations. How You Will Achieve It Identify local health care gap and improve quality of care provided to maximize product’s value and long term development in broader regions. ● Evaluate new products, new indications, new research programs, new business potentials of oncology therapeutic areas from medical perspective to support new product introduction into GE (geography expansion). ● Align with cross function team including marketing, category medical oncology team etc, develop GE -specific medical strategy and design medical projects. ● Develop and implement implementation research and publication plan. ● Evaluate and review Investigator Initiate research proposal or independent education program to ensure its scientific standard and strategy fit Partnering with PHC in quality improvement of cancer prevention and treatment ● Academic communication to enhance the delivery of new concept and Pfizer products key message to key influencers and stakeholders, and Establish Cooperation and partnership with medical association to promote medical advancement. ● Set up national level KOL database, and keep medical communication with through various approaches ● Design educational programs for top KOLs and implement them ● Support on China treatment guideline development, scientific interpretation and promotion ● Publish or facilitate publication of medical paper in professional journals ● Cooperation with local medical societies to conduct medical programs/conference to facilitate new concept and state of art medical progress’ introduction to China As a key partner to provide medical input on business decision making ● Co-develop product strategy, positioning, key message with GE Marketing team ● Provide medical support (topic design, KOL communication etc.) on key marketing activities ● Provide broad and deep medical insight/summary document of the defined therapeutic area to business partners to deal with key product/disease area issues such as NEDL, Hospital listing, new initiatives etc. ● Review and approve Local Standard Response Letter to HCPs Develop sale force’s medical capability through training program design, Lecture Delivery and periodic medical knowledge update in different settings through various channel ● At Phase I sales training ● At National sales conference ● Field visit ● Special sales force program ● Give lectures or updates to other stakeholders to increase their disease and product knowledge In order to maintain company’s image and protect patient’s welfare, MA act as a core member to work with cross function team on crisis management. ● Perform medical evaluation, explanation on the event; ● Develop medical justification or responding document. ● Provide medical expert opinion on company responding strategy ● Review and approve all external communication documents to make sure all delivered message are medically precise and consistent ● Communicate with external customers directly for medical issues as necessary 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 thestudy 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 medical compliance. ● Act as the sole reviewer to ensure educational grants within medical compliance ● Review and approve promotional materials and activities to ensure their scientific standard and medical compliance with external and internal requirements Qualifications Must-Have ● Expertise in public health or project management in health care . ● Therapeutic area knowledge: familiar with the disease knowledge and clinical practice of the therapeutic area ● Language: Fluent in English (both spoken and written) is preferred ● Primary Clinical trial knowledge ● Computer: Familiar with Microsoft Office software is preferred ● Ability to rapidly catch up global leading edge medical advancement ● Strong business acumen ● Strategic thinking and analytic skills ● Good interpersonal communication skills ● Proactive planning and result oriented ● Customer focus ● Excellent Teamwork/Collaboration ● Managerial ● Sustain Focus on Performance ● Accountability ● Manage Change ● Align Across Pfizer ● Education ● Clinical Medicine Background in the defined therapeutic area, master degree, Master above is required Nice-to-Have ● Minimum 3+years of experience of clinical practice in Tier 3 hospitals or experience in implementation research and public health projects is preferred ● Preferred experience as Medical Advisor or MSL in other multinational pharmaceutical companies or methodologist/researcher have cooperated with MNC Medical department in oncology disease area. 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)

北京東城區(qū)五礦廣場

職位發(fā)布者

劉一飛/人事經(jīng)理

剛剛活躍
立即溝通
公司Logo輝瑞投資有限公司公司標(biāo)簽
輝瑞公司(Pfizer Inc.)創(chuàng)建于1849年,總部位于美國紐約,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、安全和價值標(biāo)準(zhǔn)。我們在全球的產(chǎn)品組合包括創(chuàng)新藥品和疫苗。每天,輝瑞在發(fā)達(dá)和新興市場的員工都在推進(jìn)人類健康,推動疾病的預(yù)防、治療和治愈,以應(yīng)對挑戰(zhàn)我們這個時代的頑疾。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,輝瑞一直致力于為所有依賴我們的人帶來改變。輝瑞于1989年進(jìn)入中國市場。扎根中國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。目前輝瑞在中國業(yè)務(wù)覆蓋全國300余個城市,累計投資超過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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