职位描述
Job Responsibilities:Medical Information:
- Respond (verbal and written) to unsolicited technical/medical questions from healthcare professionals and internal customers by the retrieval, evaluation and presentation of high quality information using in-house and external sources in a timely and efficient manner
- Use and adapt global standard responses and generate new UCB China standard responses in line with the relevant SOPs
- Acquire and maintain therapy areas and products knowledge and expertise
- Contribute to internal monthly reports/metrics which includes relevant information regarding queries received and resolved within MI Department for distribution to other UCB departments
- Maintain the scientific MI platform for internal share of literatures, FAQ, Standard Documents
Pharmacovigilance:
- Manage, collect, record and file all Individual Case Safety Reports (ICSRs) received in the country on investigational drugs and marketed products according to Patient Safety SOPs, local SOPs and local Health Authorities regulations
- Provide assistance in reporting to the Regulatory Authorities, ICSRs, aggregate reports and any other information that should be reported according to internal proceedings, and local laws and regulatory requirements
- Act as backup in the absence or unavailability of the Affiliate Safety Leader or Deputy.
Admin:
- Support Safety and Medical Information department finance and administration activity such as payment, agreement archiving, meeting organization, electronic and hardcopy filing etc.
Education:
Bachelor's degree
Experience:
Previous R&D or industry experience as an advantage
企业简介
作为全球领先的生物制药公司，总部设在比利时布鲁塞的优时比（UCB）公司，秉承造福人类的使命，在近八十年的发展中，为全球重症疾病患者提供了若干独具特色的药物。优时比（UCB）公司通过采用创新的方式进行化学药品与生物药品的研究与开发，主要致力于中枢神经系统疾病，过敏/呼吸系统疾病、自身免疫疾病及肿瘤疾病的治疗领域的研究。在重症疾病治疗领域中，优时比（UCB）公司始终处于先行者的地位。在全球40多个国家拥有8,400多名员工，2006年，优时比（UCB）公司实现收入25亿欧元，优时比（UCB）公司在欧洲布鲁塞尔证券交易市场上市。
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