东莞招聘

MAIN REPONSIBILITIES / DUTIES

Maximize the value of Pfizer products to Chinese patients and health care professional within Pfizer’s vision and mission. Develop China medical development and life-cycle management strategy for inline products and pipeline within Pfizer China business objectives and strategy. Provide state of the art medical and clinical development expertise to drive Pfizer clinical trials. Establish platform and channel with China academic organization in defined therapeutic area to delivery Pfizer products message to key influencers and stakeholders. Build effective medical advisor interface and provide professional medical training to support commercial teams to achieve their objectives.

Lead and develop product life-cycle management strategy from medical perspective to maximize product’s value and long term development.

Develop and execute medical plan for the defined therapeutic area(s) aligning with products development strategy

Identify medical opportunity in current trends of diagnosis, existing/emerging treatment options , and unmet medical needs in defined therapeutic area as medical base for business initiative and decisions

Evaluate new products, new indications, new research programs, new business potentials of defined therapeutic areas from medical perspective to support business decisions

Develop post marketing research strategy based on registration/market needs in alignment with cross function team including marketing, CCO team, and global team

Evaluate and endorse phase IV study direction, and drive its endorsement from company

Oversee and manage local Non-interventional Study (NIS) study

Review and endorse Investigator Initiate research proposal to ensure its scientific standard and strategy fit

Develop and execute publication plan, provide input to the publication plan, provide ideas for generating manu"script"s of scientific interest, and actively review manu"script"s and abstracts to ensure medical and scientific accuracy

Work with BU marketing and sale leaders on therapeutic strategies and key issues resolution from medical point of view

Review and approve medical dossier for drug reimbursement listing, pricing bidding and other access related issues.

Coach and guide the team to provide medical input to MI team on LSRD

Coach the team to communicate medical update to internal and external customer and answer complicated medical queries.

Develop sale team medical capability through medical training ,lecture delivery and medical knowledge update through various channel

Coach and guide team to design/conduct effective training programs on field force supporting programs to develop sale team’s medical capability, and solve key medical issues.

Support products registration activities

Provide medical advice to registration trials protocol synopsis and study report

Review and approve of local product labeling (LPD)

Review and approve medical justification document to support LPD related queries from drug administration agency

Provide medical input in feasibility evaluation of global and local trials

Provide official input on study site selection from therapeutic prospective

Enhance the delivery of new concept and Pfizer products key message to key influencers /stakeholders, and establish cooperation and partnership with medical association to promote medical advancement

Guide team to set up top national level KOL database, and effective medical communication plan through various approaches , and ensure its implementation

Establish strategic partnership with local medical association through appropriate medical programs

Cooperate with local medical association to facilitate new concept and the state of the art medical progress

Coach and guide the team to provide medical support to China clinical practice guideline development, scientific interpretation and promotion

Act as a core member to work with cross function team on crisis management to maintain company’s image and protect patient’s welfare

Coach and develop team to perform medical evaluation, explanation on the event

Approve medical responding document

Provide medical expert opinion and guidance 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

Coach the team to 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.

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.

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

In-depth Clinical trial knowledge

Computer: Good at Microsoft Office software

Strong business acumen

Capability of strategic insight to drive new business direction from medical perspective

Cross functional leadership skill

Strong communication and influencing skill

Managerial

Sustain Focus on Performance

Create an Inclusive Environment

Encourage Open Discussion and Debate

Manage Change

Align Across Pfizer

Certifications

N/A

Education

？ Master degree major in clinical medicine, Medical doctoral degree or PHD in medical is preferred

？ Master of Business Administration is a plus

Experience

3 years clinical practice in Tier 3 hospitals (corresponding specially is preferred)

MD or PHD with 3+ years medical affairs experience in multinational pharmaceutical companies experience, or

Master with 5+ years experience, or Management experience preferred

辉瑞公司（Pfizer Inc.）创建于1849年，迄今已有160多年的历史，总部位于美国纽约，是目前全球***的以研发为基础的生物制药公司。辉瑞致力于运用创新的科学技术以及全球资源来改善每个生命阶段的健康和福祉。
我们的目标是“不断创新为患者带来能显著改善其健康的药物”。我们的使命是“成为一家卓越的创新型生物制药公司”。
2012年辉瑞公司全年合计收入590亿美元，研发投入78亿美元。辉瑞在全球拥有9万多名员工，59家生产基地，业务遍及全球150多个国家和地区。2012年财富全球500强企业中辉瑞排名126位。
目前辉瑞公司的产品覆盖了包括化学药物、生物制剂、疫苗、健康药物、动物保健品等用于人类、动物和消费者保健等诸多广泛而极具潜力的治疗及健康领域，同时其卓越的研发和生产能力处于全球领先地位。
在人类和动物药品的发现、开发和生产过程中，辉瑞始终致力于奉行严格的质量、安全和价值标准。每天，分布在世界各地的辉瑞员工致力于促进当地医疗卫生的发展以及探索能够应对当今最为棘手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承付的医疗卫生服务。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。160多年来，辉瑞一直努力为人们提供更好、更优质的服务。
辉瑞生物制药目前在华上市的创新药物已超过50个，其治疗领域涵盖了心脑血管及代谢、抗感染、中枢神经、抗炎镇痛、抗肿瘤、泌尿、疫苗及等诸多领域。其中如立普妥®、络活喜®、万艾可®、舒普深®、希舒美®、沛儿®、索坦®许多产品在市场上处于领先地位。为了让中国的广大患者能及时接受与全球同步的先进的药物治疗，辉瑞未来将进一步加大和加快在华新药引进和上市的力度和速度。
辉瑞健康药物旗下的善存®、钙尔奇®、惠菲宁®等消费保健产品也在中国市场家喻户晓，并以其优异的品质深受广大消费者的青睐；辉瑞旗下的硕腾动物保健品*为中国的动物保健市场提供各类领先的动物疫苗和动物药品。

At Pfizer, we apply science and our global resources to improve health and well-being at every stage of life. We strive to set the standard for quality, safety and value in the discovery, development and manufacturing of medicines for people and animals. Our diversified global health care portfolio includes human and animal biologic and small molecule medicines and vaccines, as well as nutritional products of healthcare industry and many of the world's best-known healthcare products such as Centrum. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as the world's leading biopharmaceutical company, we also collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 160 years, Pfizer has worked to make a difference for all who rely on us.