长沙招聘

I. Purpose of this job:
To enhance the medical competence of Clinical & Medical & Regulatory (CMR) Dept. and make biggest contribution to the business of company via clinical trial design and giving medical supports to clinical study, medical reporting, medical affairs & regulatory affairs in CMR Dept.

II. Area of responsibilities:
a)Main Tasks:
1. Responsible for phase 3 and phase 4 clinical trial/study design initiated by Novo Nordisk in align with regulatory requirement and/or marketing strategy
2. Prepare extended protocol synopsis for clinical trials and studies and prepare full protocols when necessary
3. Take medical responsibility to ensure appropriate trial execution and evaluation, e.g. medical support for investigator meeting, handling medical related issues during operation, etc.
4. Prepare relevant material to answer questions raised by HA officials and professionals from clinical point of view
5. Review labelling of new products.
6. Review and approve medical content of study reports and publications based on result of clinical studies.
7. Protocol review for investigator initiated studies
8. Provide medical expertise in a therapeutic area with focus on a specific project and be the internal spokesperson for medical aspects of a given project.
9. Responsible for preparation of high-level medical activities, e.g. external result meeting, Advisory Board meeting
10. Provide training of updated knowledge of products and diabetes to improve the internal medical capability.
11. Provide instruction and technical coaching for others for specific clinical programme

b)Supervision:
None

c)Main customers:
Internal: colleagues from CMR Dept., MKT
External: doctors and investigators, health care professionals and officials.

III. Education and Experience Requirements of the Position:
1. Master degree or above of clinical medicine
2. At least 3 years working experience as practicing physician, preferably in diabetes or with working experience in global pharmaceutical companies
3. Working experience of clinical trial is preferred
4. Have good understanding of requirements for protocol preparation
5. Have good understanding of requirements from SFDA on registration trial
6. Be good at interpersonal communication
7. Proficiency in oral and written English
8. Good computer using skills

注意事项：感谢您对诺和诺德的支持，请点击“立即申请”按钮，注册并投递简历至诺和诺德招聘网站，我们将保存您的简历至诺和诺德专业人才库中，并及时与您联系。如果您对诺和诺德招聘网站有任何问题，请您联系recruit@novonordisk.com 感谢您的支持！

　　诺和诺德是世界领先的生物制药公司，在用于糖尿病治疗的胰岛素开发和生产方面居世界领先地位。诺和诺德总部位于丹麦首都哥本哈根，员工总数30000人，分布于79个国家，产品销售遍布180个国家。在欧美均建有生产厂。
　　诺和诺德的产品60年代初就已进入中国市场。1994年初，诺和诺德董事会通过了在中国实施战略投资的计划，在北京建立诺和诺德（中国）制药有限公司总部和生物技术研究发展中心，在天津兴建现代化生产工厂，并在全国30多个城市建立了完善的营销体系。欲了解详情，请访问诺和诺德中国网站：www.novonordisk.com.cn

　　为配合公司在中国业务的迅速发展，现诚聘。

　　诺和诺德将为您提供具有竞争力的福利、完善的个人发展与培训机会，使您在国际化的管理与富有挑战性的工作环境中不断地进步与自我实现！应聘者请将个人简历、期望薪水、身份证、学历证明复印件于10日内寄至本公司。
　　请在信封上注明应聘职位。