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數(shù)據(jù)庫管理組負責人

輝瑞(中國)研究開發(fā)有限公司
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工作性質: 全職 更新日期: 07-27
專業(yè)要求: 不限 學歷要求: 本科統(tǒng)招
職稱要求: 不限 性別要求: 不限
年齡要求: 不限 經驗要求: 不限
工作地區(qū): 湖北·武漢 戶口要求: 不限
截止日期: 2025-03-13 外語要求: 不限
工資待遇: 面議 招聘人數(shù): 1人
其他福利:
崗位職責:????General?·???????????Manage?the?team?of?Database?Managers?at?Wuhan?·???????????Ensure?relevant?SOPs?and?processes?are?consistently?implemented?·???????????Monitor?and?report?on?the?progress?of?achieving?functional?area?goals?·???????????Develop?colleagues?in?the?team,?including?recruitment,?retention,?mentoring?and?performance?management?for?staff.???Specific?·???????????Ensure?that?all?techops?activities?are?conducted?in?compliance?with?applicable?Pfizer?SOPs?and?processes,?Pfizer?Data?Standards,?as?well?as?relevant?regulatory?requirements.??·???????????Partner?with?CDS?peers?to?implement?strategies?to?ensure?on?time?delivery?and?high?quality?in?Database?Build,?CRF?Design,?Data?Acquisition,?PK/PD,?Medical?Labs,?Coding?and?Data?Processing?from?study?set-up?to?database?release.?·???????????Manage?the?DBM?team?to?meet/exceed?CDS?metrics?and?study?specific?goals.??·???????????Work?with?peers?to?resolve?cross-functional?barriers?that?prevent?achieving?data?management?milestones.?·???????????Ensure?appropriate?resources?are?identified?and?allocated?to?support?assigned?studies?and?tasks.?·???????????Actively?participate?in?project?review?meetings.??·???????????Develop?and?maintain?charters,?resource?utilization?metrics?and?project?plans.???·???????????Partner?with?peers?to?promote?initiatives?in?improving?work?efficiency.???任職要求:?·?????????Customer?Support?experience:?Demonstrated?knowledge?and?success?in?supporting?external?and/or?internal?customers?in?a?clinical?development?environment.?·?????????Site/Team?Management?experience:?Previous?people?management?experience?is?strongly?preferred.?·?????????Process?improvement/tracking:?Demonstrated?capability?in?developing?tracking?tools?to?manage?and?evaluate?workflow?and?workload.??Ability?to?evaluate?data?and?change?processes?as?necessary?for?efficient?use?of?personnel?and?resources.?·?????????Project/process?management:?Experienced?in?managing?complex?projects?and?processes?·?????????Clinical?&?regulatory?processes:?Demonstrated?knowledge?in?clinical?development,?ICH/GCP?and?regulatory?requirements?·?????????Scientific/administrative?excellence:?Demonstrated?success/results?in?prior?scientific/administrative?management?roles?·?????????Systems?Technologies:?Knowledge/understanding?in?technologies?to?support?clinical?data?acquisition,?data?validation?and?data?collection;?strong?understanding?of?the?state-of-the-art?clinical?data?management?technologies?to?evaluate?and?leverage?them?into?improved?business?processes?for?worldwide?deployment?and?adoption?·?????????Presentation/influencing?skills:?Demonstrated?platform?skills;?experience?presenting?to?large?scientific?audiences?and?non-science?populations?·?????????Budget?/?expense?management:?Understands?and?has?demonstrated?ability?to?manage?budget;?history?of?staying?on?or?under?budget?·?????????Proven?strong?supervisory?and?leadership?skills:?Demonstrated?ability?to?manage?a?team?of?clinical?professionals.?Transparent?skills?in?providing?vision,?direction?and?leadership?to?a?group?of?individuals?with?different?levels?of?experiences.?·?????????Minimum?of?a?B.S.?degree?in?either?scientific?or?medicinal?related?field,?e.g.?clinical?medicine,?pharmacology,?or?other?life?science?majors.?·?????????Advanced?degree?is?preferred.?·?????????Demonstrated?knowledge?on?drug?development?and?clinical?trial?operations?with?thorough?understanding?and?extensive?experience?in?clinical?data?management.??·?????????Comprehensive?technical?capability?in?applying?clinical?trial?database?and?applications?in?implementing?CRF?design,?clinical?database?set?up,?data?review,?query?resolution,?reporting,?etc.??·?????????Demonstrated?success?in?managing?multiple?clinical?programs?and?complex?projects?and?timely?delivering?high?quality?results.??·?????????Previous?experience?leading?a?substantial?group?responsible?for?clinical?data?management,?clinical?study?management,?or?equivalent?function?in?clinical?operations.???·?????????Demonstrated?leadership?behaviors?and?resource?management?(staff?and?financial)?skills.?·?????????Strong?negotiation?and?conflict?resolution?skills?are?essential.??Ability?to?remain?focused?in?high-stress?situation?is?very?important.??·?????????Proven?history?of?success?in?building?strong?customer?relationships.?·?????????Effective?verbal?and?written?communication?in?English.??An?international?experience?is?a?plus.

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日宣布輝瑞中國研發(fā)中心正式在上海揭幕。輝瑞中國研發(fā)中心主要為全球輝瑞藥物開發(fā)提供支持工作。大部分的功能是圍繞在I-IV期臨床試驗研究設計、數(shù)據(jù)管理和生物統(tǒng)計分析、以及臨床試驗報告的部分準備工作。此外,該中心是輝瑞全球安全和風險管理部的一個分支,負責安全數(shù)據(jù)處理和評估工作。研發(fā)中心還將為輝瑞公司在中國及亞洲的其它運營部門的員工提供國際標準的臨床試驗管理規(guī)范(GCP)的技術培訓。
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數(shù)據(jù)庫管理組負責人 面議
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