職位描述
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
企業簡介
作為全球領先的生物制藥公司，總部設在比利時布魯塞的優時比（UCB）公司，秉承造福人類的使命，在近八十年的發展中，為全球重癥疾病患者提供了若干獨具特色的藥物。優時比（UCB）公司通過采用創新的方式進行化學藥品與生物藥品的研究與開發，主要致力于中樞神經系統疾病，過敏/呼吸系統疾病、自身免疫疾病及腫瘤疾病的治療領域的研究。在重癥疾病治療領域中，優時比（UCB）公司始終處于先行者的地位。在全球40多個國家擁有8,400多名員工，2006年，優時比（UCB）公司實現收入25億歐元，優時比（UCB）公司在歐洲布魯塞爾證券交易市場上市。
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