崗位職責(zé):
? Monitor and distribute regulatory regulations/guidelines and other information related to drug development and regulatory activities. Maintain an effective Regulatory Intelligence database.
? Lead or coordinate the collection comments of draft regulations/guidelines and provide feedback to trade associations or Health Authorities.
? Lead or coordinate learning and assessment on the business impact of regulations and guidelines.
? Support the preparation of talking points and slides for external meetings and visit.
任職要求:
? Master’s degree.
? At least two years of relevant work experience in the pharmaceutical field, with a preference for those with a background in regulatory affairs.
? Excellent interpersonal and communication skills and the ability to work effectively.
? Proficient in computer skills, especially PPT.
? Good command of English skill, oral and written.
? Execution for assigned projects.
核心工作職責(zé)
? 監(jiān)控并分發(fā)與藥物開發(fā)和監(jiān)管活動相關(guān)的監(jiān)管法規(guī)/指南及其他信息。維護(hù)有效的監(jiān)管情報數(shù)據(jù)庫。
? 主導(dǎo)或協(xié)調(diào)收集對法規(guī)/指南草案的意見,并向行業(yè)協(xié)會或衛(wèi)生當(dāng)局提供反饋。
? 主導(dǎo)或協(xié)調(diào)對法規(guī)和指南對業(yè)務(wù)影響的學(xué)習(xí)和評估。
? 為外部會議和訪問準(zhǔn)備發(fā)言要點和幻燈片。
資格要求與必備經(jīng)驗與技能
? 碩士學(xué)位。
? 至少兩年制藥領(lǐng)域相關(guān)工作經(jīng)驗,有監(jiān)管事務(wù)背景者優(yōu)先。
? 出色的人際交往和溝通能力,以及有效工作的能力。
? 熟練掌握計算機(jī)技能,尤其是PPT制作。
? 英語聽說讀寫能力強(qiáng)。
? 能夠執(zhí)行分配的項目。
其他要求
? 具備戰(zhàn)略思維、領(lǐng)導(dǎo)力和快速學(xué)習(xí)能力。