更新于 12月26日

医学部 -(高级)医学顾问-广阔市场

1-2万
  • 北京东城区
  • 3-5年
  • 大专
  • 全职
  • 招1人

雇员点评标签

  • 同事很nice
  • 团队执行强
  • 工作环境好
  • 人际关系好
  • 氛围活跃
  • 实力大公司

职位描述

医药代表
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

工作地点

北京东城区五矿广场

职位发布者

王先生/区域招聘及入职交付

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辉瑞公司(Pfizer Inc.)创建于1849年,总部位于美国纽约,是一家以科学为基础的、创新的、以患者为先的生物制药公司。辉瑞的使命是“为患者带来改变其生活的突破创新”。在辉瑞,我们通过科学和全球资源为人们提供治疗方案,以延长其生命,显著改善其生活。在医疗卫生产品的探索、研发和生产过程中,辉瑞始终致力于奉行严格的质量、安全和价值标准。我们在全球的产品组合包括创新药品和疫苗。每天,辉瑞在发达和新兴市场的员工都在推进人类健康,推动疾病的预防、治疗和治愈,以应对挑战我们这个时代的顽疾。辉瑞还与医疗卫生服务方、政府和社区合作,支持并促进世界各地的人们能够获得更为可靠和可承付的医疗卫生服务。这与辉瑞作为一家全球卓越的创新生物制药公司的责任是一致的。170余年来,辉瑞一直致力于为所有依赖我们的人带来改变。辉瑞于1989年进入中国市场。扎根中国30余年,辉瑞已成为在华主要的外资制药公司之一。2021年是辉瑞新征程的开始。迄今已有170余年历史的辉瑞正在迈入全新时代,成为一家以科学为基础的、创新的、以患者为先的生物制药公司。目前辉瑞在中国业务覆盖全国300余个城市,累计投资超过15亿美元,并设立了1家先进的生产设施,2个研发中心(分别位于上海张江高科技园区和武汉光谷),在华有近7,000名员工分布于业务、研发和生产等领域。辉瑞在华上市了五大领域的高品质创新产品,包括肿瘤、疫苗、抗感染、炎症与免疫、罕见病等多个领域的处方药和疫苗,强大完善的产品线旨在满足生命各阶段的健康需求。
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