东莞招聘

工作职责:

MAIN REPONSIBILITIES / DUTIES

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 etc, develop post marketing research strategy based on Registration/Market needs

？ Provide phase IV study direction and develop key elements

？ Design and manage local Non-interventional Study (NIS) study as a clinician.

？ Develop medical strategy and implement it to support product development

？ Develop publication plan and implement it

？ Evaluate and review Investigator Initiate research proposal to ensure its scientific standard and strategy fit

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

？ Provide broad and deep medical insight/summary document of the defined therapeutic area to business partners to deal with key product issues such as bidding, RDL, new initiatives etc.

？ 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 prospective

？ 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. 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

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).

？ 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 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 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.

8. 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

任职资格:

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 softwares

？ 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

Certifications

N/A

? Education

？ Medical or pharmaceutical Background, Master Degree or above, Ph D or MD in the defined therapeutic area is preferred

? Experience

？ About 3 years clinical practice or medical affairs experience in other multinational pharmaceutical companies

？ Good medical knowledge in the defined therapeutic area

？ Good understanding about pharmaceutical business, Medical affairs experience or clinical studies experience in multinational pharmaceutical companies

？ Proficiency in English and good computer usage

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.