延吉招聘

? Perform Medical Information activities in line with Core Global Medical Information (MI) Standards sop-008513.

? Perform Medical Information activities in compliance of global and local requirements and regulations.

? Maintain daily management of the Affiliate Medical Information mailbox to ensure that all spontaneous MI enquiries are processed accordingly.

? Maintain daily management of the Global MIS by logging in on a regular basis during the working day.

? Create and maintain all documentation related to Medical Information Enquiry quality checking accordingly to standard operating procedure-associated instruction, associated form and guidance document.

? Conduct periodic Reconciliation accordingly to standard operating procedure-associated instruction for Medical Information Reconciliation with Patient Safety and Quality Assurance and associated form.

? Comply with the Content Management as per standard operating procedure-associated instruction for Global Products and guidance document.

? Participate in preparation, review and maintenance of all medical information Standard Response Documents (SRDs) and Frequently Asked Questions (FAQs) for assigned product(s) in line with sop-ai (per local Medical Information set-up).

? Provide regular updates and reporting related to Medical Information activities at Affiliate level.

? Regularly liaise with Global Medical Information and cross-functional stakeholders e.g Patient Safety, Quality Assurance, Regulatory Affairs.

Education Level：

Bachelor's Degree

Master's Degree

Ph.D.

Law (J.D.)

Medical Degree (M.D.)

Other (Describe):

Other Certification：

Certification (Describe):

Registration (Describe):

Licensure (Describe):

Other (Specify):

Experience：

? 2 -3year/s experience in the bio-pharmaceutical industry within MI/MI of a multi-national bio-pharmaceutical company

? Mandatory - Undergraduate or post-graduate education in science related disciplines

COMPETENCIES：

? Ability to understand various key stakeholders and customers to respond appropriately

? Proficiency in use of PC applications

? Ability to manage and meet deadlines

? Ability to work effectively in a team environment.

? Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives.

? Excellent verbal and written communication in English.

? Demonstrated ability to understand, analyze, and summarize scientific and medical information.

? Professional demeanor, team orientated, self-motivated, and ability to influence customers both externally and internally.

比利时优时比制药公司（UCB）始建于1928年，总部设在比利时布鲁塞尔，在英国伦敦Slough和剑桥等地拥有2个研发中心。在八十年的发展中，优时比制药公司致力于为重症患者提供更多的创新治疗方法，造福人类。 优时比制药在全球业务遍布40多个国家，拥有近一万名员工。2010年全球销售收入32亿欧元。全球百强医药行业排名第33位。随着业务的不断拓展，2004年5月，优时比制药完成了对英国生物制药企业--细胞技术公司的收购。2007年9月1日，又完成了对德国许瓦兹制药集团的全球并购。至此，优时比制药公司成功地实现了全球领先的生物制药公司的战略定位。
优时比制药在华机构包括优时比贸易（上海）有限公司和珠海许瓦兹制药有限公司，业务遍及全国，产品涉及中枢神经系统疾病、变应性疾病、心血管疾病、贫血和疼痛治疗等领域。
创新、开拓、诚信、尽责、关爱、包容与业绩是优时比制药公司始终遵循的价值观。
面向未来，比利时优时比制药公司一如既往地秉承特有的业绩、尽责、诚信、包容、关爱、开拓和创新的价值观和企业文化，将建设一个全球生物医药的领先者，首要任务是带来专家和新药，治疗各种严重疾病的患者。
    
公司网站：******************
中文网站：************************

为什么选择我们？

卓越完善的人才发展战略
优时比业务的多样性和国际化为其员工提供了广阔的个人发展平台。员工一旦加入我们，就会得到公司在培训、业绩表现和个人潜力挖掘等方面提供的帮助。无论您的专业和职务是什么，您都将对自己的发展前景了然于胸。我们不仅提供正规的培训，而且还通过精良的个人发展计划和在职培训等途径为您的前途指路。

有竞争力的薪酬体系
从长远来看，为了吸引人才，保留人才，并激励人才，我们确保所提供的薪资福利具有市场竞争力。我们期待着员工能有优秀的表现并得到优厚的回报，因而把薪资和员工对公司的贡献直接联系起来。
上海总公司地址：上海市西藏中路268号来福士广场办公楼2802室

欢迎有意向的候选人可将简历投递至邮箱：chinacampus@ucb.com。应聘简历请在主题中注明申请职位名称。