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            更新于 4月8日

            Sr. Medical Advisor

            2.5-3.5萬
            • 北京東城區
            • 3-5年
            • 碩士
            • 全職
            • 招1人

            雇員點評標簽

            • 同事很nice
            • 團隊執行強
            • 工作環境好
            • 人際關系好
            • 氛圍活躍
            • 實力大公司

            職位描述

            生物藥
            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. 1. Enhance local data generation and Product life-cycle management from medical perspective to maximize product’s value and long-term development ● Evaluate new products, new indications, new research programs, new business potentials of defined therapeutic areas from medical perspective to support new product introduction and line extension ● Align with cross function team including marketing, CCO team, global team et al, develop post marketing research strategy based on Registration/Market needs ● Provide phase IV study direction and develop key elements 2. As a key partner to provide medical input on business decision making ● Co-develop product strategy, positioning, key message with Marketing team ● Provide medical support (topic design, KOL communication etc.) on key marketing activities ● Review and approve Local Standard Response Letter to HCPs 3. 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 4. Support Drug Registration Activities ● Timely review and approval of local product labeling (LPD) ● Develop medical justification document to support LPD related queries from government ● Provide medical input in feasibility evaluation of studies for global trials ● Provide official input on study site selection from therapeutic perspective ● Provide input to registration protocol synopsis and study report as necessary 5. 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 6. 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 7. 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). 8. Ensure company’s medical compliance. ● Act as the sole reviewer to ensure educational grants within medical compliance ● Support in review and approval of promotional materials and activities to ensure their scientific standard and medical compliance with external and internal requirements REQUIRED SKILL SET Technical ● Therapeutic area knowledge: familiar with the disease knowledge and clinical practice of the therapeutic area ● Language: Fluent in English (both spoken and written) ● Primary Clinical trial knowledge ● Computer: Familiar with Microsoft Office software ● 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 preferred Experience ● 3 years clinical practice in Tier 3 hospitals (corresponding specialty is preferred) or medical affairs experience in other multinational pharmaceutical companies

            工作地點

            北京東城區五礦廣場

            職位發布者

            劉一飛/人事經理

            當前在線
            立即溝通
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            輝瑞公司(Pfizer Inc.)創建于1849年,總部位于美國紐約,是一家以科學為基礎的、創新的、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新”。在輝瑞,我們通過科學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。在醫療衛生產品的探索、研發和生產過程中,輝瑞始終致力于奉行嚴格的質量、安全和價值標準。我們在全球的產品組合包括創新藥品和疫苗。每天,輝瑞在發達和新興市場的員工都在推進人類健康,推動疾病的預防、治療和治愈,以應對挑戰我們這個時代的頑疾。輝瑞還與醫療衛生服務方、政府和社區合作,支持并促進世界各地的人們能夠獲得更為可靠和可承付的醫療衛生服務。這與輝瑞作為一家全球卓越的創新生物制藥公司的責任是一致的。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,成為一家以科學為基礎的、創新的、以患者為先的生物制藥公司。目前輝瑞在中國業務覆蓋全國300余個城市,累計投資超過15億美元,并設立了1家先進的生產設施,2個研發中心(分別位于上海張江高科技園區和武漢光谷),在華有近7,000名員工分布于業務、研發和生產等領域。輝瑞在華上市了五大領域的高品質創新產品,包括腫瘤、疫苗、抗感染、炎癥與免疫、罕見病等多個領域的處方藥和疫苗,強大完善的產品線旨在滿足生命各階段的健康需求。
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