上海招聘

工作职责:

Maximize the value of Pfizer products to Chinese patients and health care professional through medical activities in regional level. Lead the management and communication of product information with health-care providers, payers, and other medically-focused customers to meet Pfizer Medical Needs across our Medicines’ Lifecycles. Implement medical/research/disease management programs; introduce new concept through medical education to help doctors to improve patients’ outcome; conduct medical to medical communication to transport product knowledge and therapeutic update to key influencers and stakeholders; and Provide professional medical training to commercial teams.

1.Implementation medical programs and activities in fields

*Support Pfizer sponsored Non interventional study and other medical programs at regional level.

*Design and conduct disease management program according to timeline and with good quality.

*Provide appropriate support of Investigator-Initiated Research (IIR), such as discuss research concept with interested researcher, and communicated the nature and requirement of Pfizer’s IIR etc.

*Gain feedback and customer insights from HCPs and other customers to inform Pfizer’s development program.

*Facilitate submission of investigator initiated pre-clinical and clinical proposals, and act as a Liaison between Pfizer and IIR researcher; and follow up IIR on its progress according to timeline

2.Lead medical to medical communication in the fields

*Organize regional level medical to medical meeting and activities with KOLs to deliver cutting edge medical information of defined therapeutic area and assigned products

*Conduct medical educational meeting to introduce new concept to help doctors to improve patients’ outcome and advance their research capability

*Set up KOL database in responsible region and conduct regular medical communication.

*Provide timely feedback of KOL’s comments and insight to supervisors and relevant medical advisors

*Respond medical inquiries as needed.

*Establish good academic relationship with regional academic origination at defined therapeutic area.

*Cooperate and align with medical advisors to engage KOLs

3.Improve sale team medical ability through medical training ,lecture delivery and medical knowledge

*Orgnize face to face meeting or Webex meeting to cadcade medical information to improve sale team’s medical ability

*Present at POA and regional sales meetings for medical information

*Provide training to commercial colleagues on Pfizer medicines, disease states, health trends and channels, pharmacoeconomics, environment, or other areas of interest.

4.Medical input to product medical and brand plan

*Collect, analyze and report timely local customer medical insights to input on product strategy and message development

*Work with (Senior) medical advisor and product manager proactively to assist product strategy implementation

5.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 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 SAF 09 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

6.Ensure company’s medical compliance

*Implement medical programs and activities within medical compliance

*Comunicate medical information with compliance

*Ensure timely SOP learning, and daily practice compliant with SOPs.

任职资格:

1.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

2.Managerial

*Sustain Focus on Performance

*Create an Inclusive Environment

*Encourage Open Discussion and Debate

*Manage Change

*Develop People

*Align Across Pfizer

3.Certifications

N/A

4.Education

*Medical Background, Master Degree or above in the defined therapeutic area is preferred

5.Experience

*At least 2 years clinical practice experience in defined area with good medical knowledge

*Good understanding about pharmaceutical business, Medical affairs experience or clinical studies experience in multinational pharmaceutical companies is preferred

*Clinical research experience is preferred

*Proficiency in English and good computer usage

在辉瑞，我们致力于运用科学以及我们的全球资源来改善每个生命阶段的健康状况。在药品的探索、开发和生产过程中，我们致力于设定品质、安全和价值标准。我们多样化的全球医药产品包括生物药品、小分子药品和疫苗，以及许多世界驰名的消费产品。每天，世界各地的辉瑞员工致力于寻找我们这个时代最为棘手的疾病的预防和治疗方案。辉瑞还与世界各地的医疗卫生专业人士、政府和社区合作，支持世界各地的人们能够获得更为可靠和可负担的医疗卫生服务。这与辉瑞作为一家世界领先的生物制药公司的责任是一致的。

为了践行上述诺言，辉瑞创建了新的业务机构-辉瑞Upjohn. 辉瑞Upjohn 兼具创业公司的敏捷性、以及全球财富百强企业的资源和能力。因此，我们在创新与快速执行方面拥有独特的优势，包括激活我们的研发产品线、提高生产效能，以及快速推进产品研发等方面。

在辉瑞 Upjohn，我们相信，建立审慎的合作伙伴关系和开展协同合作，对创建可持续的医疗卫生解决方案至关重要。我们热切希望成为非传染性疾病(NCD)防治领域的***合作伙伴。由于中国市场与日俱增的重要性和机遇，同时为了确保我们能有效制定正对当地需求的健康解决方案 - 辉瑞 Upjohn高层管理团队的一些重要成员(每位都有20多年行业经验)和大部分部门都将在中国工作。这将使辉瑞 Upjohn真正实现本地化，并具备必要的速度和灵活性，从而在保持同辉瑞相关组织强有力联系的同时，切实抓住各种增长机遇。