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更新于 8月7日
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舉報

醫(yī)學(xué)寫作編輯

1.8-2.2萬
  • 上海黃浦區(qū)
  • 3-5年
  • 本科
  • 全職
  • 招999人

職位描述

臨床醫(yī)學(xué)編輯
崗位職責(zé):
?Writes, reviews, and edits scientific manuscripts, clinical study reports, plan outlines, protocols, documents for regulatory submissions, investigator brochures, posters, newsletters, or other clinical and regulatory documents
?Interprets non-clinical and clinical data in the preparation of various technical reports
?Perform literature searches and reviews
?Leads project teams in drafting individual report specifications, medical writing, and coordination of data analysis
?Schedules and conducts peer and team quality control review for assigned projects
?Serves as primary functional representative on project teams
?Provides both in-house and outside consulting services
?Reviews all relevant documents and interacts with functional leader and project manager to develop a thorough understanding of project timelines
?Contributes to clinical protocol development
?Performs other tasks as directed by the line manager
任職要求:
?A post graduate degree from an accredited institution in Life Sciences or Health-related Sciences, or equivalent
?Science or medical related writing experience required
?Familiarity with medical terminology
?Experience using computerized systems (PC-Windows and MS Word)
?Excellent written, oral communication and presentation skills
?Fluent in English reading, writing and speaking
?Pharmaceutical company or CRO experience developing pharmaceutical drugs for human use (e.g. pre-clinical science, medical related writing, clinical trials management, monitoring, or as an investigator or study coordinator for clinical trials)
?Experience in clinical study design and protocol development/writing
?Knowledge of regulatory submissions requirements, ICH clinical study report writing guidelines
【主要負(fù)責(zé)FDA遞交，英語要求流利】

工作地點(diǎn)

上海黃浦區(qū)Soho復(fù)興廣場

職位發(fā)布者

顧意蓉/高級人力資源專員

昨日活躍
立即溝通
公司Logo上?？档潞胍磲t(yī)學(xué)臨床研究有限公司
康德弘翼（WuXi Clinical），是藥明康德（WuXi AppTec）的一家全資子公司。始終致力為全球客戶提供全方位的臨床研究服務(wù)，包括藥品、生物制品、醫(yī)療器械、體外診斷試劑等醫(yī)藥產(chǎn)品，涵蓋BE(Bioequivalence)/ I期至IV期的臨床試驗。通過嚴(yán)格的質(zhì)量控制體系和專業(yè)團(tuán)隊的豐富經(jīng)驗，幫助創(chuàng)新性，突破性醫(yī)藥產(chǎn)品盡快上市和造?；颊?。康德弘翼立足中國，面向世界，以上海總部為中心，輻射全球制藥公司、生物技術(shù)公司以及醫(yī)療器械公司。目前，公司實行全球聯(lián)合運(yùn)營，人員規(guī)模達(dá)850+人，運(yùn)營能力覆蓋中國、美國及澳大利亞等，并在上海、北京、廣州、武漢、成都、長沙、西安、沈陽、中國臺北、美國奧斯汀、美國圣地亞哥和澳大利亞悉尼等地均設(shè)有辦公室。公司團(tuán)隊與各研究中心建立了良好的合作關(guān)系，始終保持著緊密的業(yè)務(wù)交流，保證了項目能高效、高質(zhì)地完成。隨著業(yè)務(wù)能力和業(yè)務(wù)范圍的不斷拓展，康德弘翼進(jìn)一步完善和增強(qiáng)了全球一體化研發(fā)服務(wù)平臺的綜合實力，助力全球創(chuàng)新合作伙伴更好、更快地開發(fā)醫(yī)藥產(chǎn)品。
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