黄色app有哪些_男人女人爽爽视频_99久久狠狠丁香综合伊人_欧美久久久久久久久_亚洲一区二区三区日韩91

招賢納士網(wǎng) 招賢納士網(wǎng)聯(lián)盟網(wǎng)站

業(yè)務(wù)系統(tǒng)高級(jí)分析員

輝瑞(中國(guó))研究開(kāi)發(fā)有限公司
分享到:
薪資面議
工作性質(zhì): 全職 更新日期: 該職位已過(guò)期
專(zhuān)業(yè)要求: 不限 學(xué)歷要求: 本科統(tǒng)招
職稱(chēng)要求: 不限 性別要求: 不限
年齡要求: 不限 經(jīng)驗(yàn)要求: 1年以上
工作地區(qū): 上海 戶口要求: 不限
截止日期: 該職位已過(guò)期 外語(yǔ)要求: 不限
工資待遇: 面議 招聘人數(shù): 1人
其他福利:
五險(xiǎn)一金 免費(fèi)班車(chē) 交通補(bǔ)貼 年終獎(jiǎng)金 專(zhuān)業(yè)培訓(xùn) 通訊補(bǔ)貼 定期體檢
Position?Purpose
Individual?filling?the?position?are?responsible?for?the?project?management?of?safety?aggregate?reports?submitted?to?regulators?that?include?the?FDA?and?EMA.??The?incumbent?will?partner?with?various?colleagues?from?safety,?clinical,?regulatory?and?other?functional?lines?to?produce?the?aggregate?reports?and?ensure?that?these?reports?are?completed?in?a?timely?manner?meeting?regulatory?compliance.
Primary?Responsibilities
? Lead?report?preparation?from?prep?to?submission?with?key?stakeholders/contributors?within?Clinical,?Regulatory,?Safety,?DevOps,?Submissions,?etc.
? Review?data?to?ensure?consistency?between?various?contributors.
? Compile?the?information?for?reports?using?various?electronic?tools?and?document?management?system.
? Coordinate?the?review?and?approval?of?the?report?and?address?review?comments.
? Ensure?reports?are?completed?prior?to?regulatory?due?date?to?meet?compliance.
? Provide?guidance?to?contributor?regarding?report?requirements.
? Participate?projects?or?subject?matter?tasks?that?support?the?group?and?deliverables.
? Participate?in?developing?and?performing?User?Acceptance?Testing?(UAT)?as?required.
? Complete?training?in?accordance?with?Pfizer’s?and?WSR?Safety?information?Management?curriculum.
Technical?Skill?Requirements
? Experience?in?the?pharmaceutical?industry,?clinical?research,?or?healthcare?related?field.
? Experience?with?Microsoft?word?&?excel,?Adobe?acrobat,?ISI?Toolbox,?etc.
? Experience?with?SharePoint?technology?(e.g.,?Microsoft?InfoPath,?SharePoint?Designer,?etc.)
? Business?Objects?experience?is?a?plus.
Qualifications?(i.e.,?preferred?education,?experience,?attributes)
? Bachelor’s?Degree?in?life?sciences,?healthcare,?or?pharmaceutical?discipline?required.
? Excellent?English?verbal,?written?communication?and?presentation?skills?required.
? Must?be?detailed?oriented.
? Strong?project?management?and?issue?resolution?skills?required.
? Demonstrated?ability?to?perform?in?a?cross-functional?environment.
? Knowledge?of?regulatory/safety?regulations?and?guidelines?desired.

On?October?31,?2005,?Pfizer?announced?the?official?opening?of?China?Research?and?Development?Center?(CRDC)?in?Shanghai.?Pfizer?Global?Research?and?Development’s?Center?is?mainly?engaged?in?drug?development?activities.?Much?of?the?facilitys?capacity?is?devoted?to?the?study?design,?data?management?and?statistical?analysis?of?global?phase?I-IV?clinical?trials,?as?well?as?the?clinical?study?report?process.?In?addition,?CRDC?is?a?part?of?Pfizer?global?Safety?and?Risk?Management?and?covers?the?functions?of?safety?data?processing?and?assessment.?The?center?also?trains?Pfizer?employees?in?China?and?throughout?the?Asia?region?in?internationally?recognized?Good?Clinical?Practice?standards.
輝瑞公司于2005年10月31日宣布輝瑞中國(guó)研發(fā)中心正式在上海揭幕。輝瑞中國(guó)研發(fā)中心主要為全球輝瑞藥物開(kāi)發(fā)提供支持工作。大部分的功能是圍繞在I-IV期臨床試驗(yàn)研究設(shè)計(jì)、數(shù)據(jù)管理和生物統(tǒng)計(jì)分析、以及臨床試驗(yàn)報(bào)告的部分準(zhǔn)備工作。此外,該中心是輝瑞全球安全和風(fēng)險(xiǎn)管理部的一個(gè)分支,負(fù)責(zé)安全數(shù)據(jù)處理和評(píng)估工作。研發(fā)中心還將為輝瑞公司在中國(guó)及亞洲的其它運(yùn)營(yíng)部門(mén)的員工提供國(guó)際標(biāo)準(zhǔn)的臨床試驗(yàn)管理規(guī)范(GCP)的技術(shù)培訓(xùn)。
聯(lián)系方式正在加載中......
掃碼關(guān)注微信公眾號(hào)
ICO 招賢納士網(wǎng) 深圳市順發(fā)網(wǎng)絡(luò)科技有限公司©版權(quán)所有 粵ICP備08108254號(hào)
業(yè)務(wù)系統(tǒng)高級(jí)分析員 面議
點(diǎn)擊隱藏
公眾號(hào)
求職招聘更方便
微信群
隨時(shí)隨地找工作
企業(yè)咨詢
為企業(yè)提供招聘服務(wù)
個(gè)人咨詢
為個(gè)人提供求職服務(wù)