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職位描述：

崗位職責(zé)：
1、負(fù)責(zé)新項(xiàng)目的開拓；
2、負(fù)責(zé)項(xiàng)目部組織協(xié)調(diào)工作；
3、負(fù)責(zé)與甲方、監(jiān)理、政府部門等工作對(duì)接，工作協(xié)調(diào)。
4、負(fù)責(zé)項(xiàng)目部崗位人員的管理工作；
5、負(fù)責(zé)組織、協(xié)調(diào)、管理分包及外部生產(chǎn)資源；
6、負(fù)責(zé)進(jìn)度款、結(jié)算款的催辦工作；
7、負(fù)責(zé)項(xiàng)目安全、質(zhì)量、文明施工、工程進(jìn)度、材料管理、成本控制等全面管控；
8、有組織能力有大局觀，有可靠的管理團(tuán)隊(duì)及分包、班組能力；
9、有一定學(xué)習(xí)能力和執(zhí)行力；
10、認(rèn)同企業(yè)文化，遵守企業(yè)規(guī)章制度。
任職要求：
1、工程相關(guān)專業(yè)大專以上；
2、計(jì)算機(jī)辦公軟件應(yīng)用操作熟練；
3、工程相關(guān)專業(yè)技術(shù)過硬，8年以上工程行業(yè)施工管理經(jīng)驗(yàn)；5年以上同崗位工作經(jīng)驗(yàn)；
4、必須具備二級(jí)建造師以上證書及中級(jí)以上職稱；具有一級(jí)建造師、高級(jí)職稱優(yōu)先；
5、應(yīng)變能力強(qiáng)，表達(dá)能力強(qiáng)，具有較強(qiáng)的溝通能力和社交技巧，具有親和力；
6、有團(tuán)隊(duì)協(xié)作精神，善于挑戰(zhàn)。
工作地：項(xiàng)目所在地

職位描述：

崗位職責(zé)：

1、全面負(fù)責(zé)物業(yè)項(xiàng)目的日常運(yùn)營管理工作，保證項(xiàng)目管理規(guī)章制度、工作程序的嚴(yán)格執(zhí)行，保證項(xiàng)目各項(xiàng)工作業(yè)務(wù)品質(zhì)達(dá)到公司目標(biāo)要求；

2、全面主持項(xiàng)目物業(yè)管理處的工作，對(duì)物業(yè)管理處的運(yùn)營、人事、財(cái)務(wù)、資產(chǎn)等各方面管理負(fù)全權(quán)責(zé)任；

3、負(fù)責(zé)組建管理團(tuán)隊(duì)，擬定各崗位工作規(guī)范，組織進(jìn)行管理行業(yè)知識(shí)及業(yè)務(wù)技能培訓(xùn)；

4、組織制定本項(xiàng)目預(yù)算和預(yù)算控制工作，監(jiān)督內(nèi)部費(fèi)用的合理使用和支出，在滿足服務(wù)需求的前提下，開源節(jié)流，完成項(xiàng)目經(jīng)營管理目標(biāo)；

5、協(xié)調(diào)下屬部門的關(guān)系，組織協(xié)調(diào)本項(xiàng)目內(nèi)外業(yè)務(wù)關(guān)系，對(duì)突發(fā)事件進(jìn)行及時(shí)有效的處理；

6、負(fù)責(zé)本項(xiàng)目各項(xiàng)指標(biāo)的完成，并組織好全過程的預(yù)防、控制性工作；

7、負(fù)責(zé)質(zhì)量計(jì)劃的實(shí)施和落實(shí)質(zhì)量責(zé)任制，負(fù)責(zé)落實(shí)安全責(zé)任制；

8、負(fù)責(zé)公司對(duì)本項(xiàng)目所簽定的各項(xiàng)指標(biāo)的完成落實(shí)。

任職資格：

1、大專以及上學(xué)歷；

2、3年及以上物業(yè)管理項(xiàng)目經(jīng)理經(jīng)驗(yàn)；

3、熟悉物業(yè)管理作業(yè)流程，全面掌握物業(yè)管理知識(shí)；

4、工作態(tài)度積極，認(rèn)真負(fù)責(zé)，能夠適應(yīng)較復(fù)雜的工作壓力和具有良好的服務(wù)意識(shí)及團(tuán)隊(duì)合作意識(shí)；

5、身高175及以上。

職位福利：五險(xiǎn)一金、年底雙薪、節(jié)日福利、高溫補(bǔ)貼、餐補(bǔ)、周末雙休

職位亮點(diǎn)：平臺(tái)實(shí)力強(qiáng)，晉升機(jī)會(huì)多，管理體系完善

職位描述：

Why Patients Need YouPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.What You Will AchieveIt is our mission to strengthen the oversight of our clinical data through stronger ownership, control, and visibility of our clinical data. You will play an important role in processing, reviewing, and receiving patient data and records. You will be organizing clinical data forms from therapeutic groups and outside investigators. You will ensure that accurate, timely, and consistent clinical data reaches the medical department and other groups. You will be relied on for data management plans including data preparation, data validation activities, etc.As a Manager, you provide guidance to operational teams for managing projects. Your planning skills will help in preparing forecasts for resource requirements, and providing areas of improvement for products, processes or services. Through your comprehensive knowledge of principles, concepts and theories of the discipline, you will also work towards advancing new concepts and methodologies. You will be able to take a leadership role to facilitate agreements between different teams.It is your dedication and focus that will help make Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve ItProvide guidance, lead/co-lead projects, manage own time to meet objectives, plan resource requirements for projects across the division.Ensure work carried out by providers is in accordance with applicable Standard Operating Procedures (SOPs) and working practices.Promote the use of consistent, efficient, and quality processes to meet timelines and deliverables.Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all Data Monitoring and Management (DMM) activities and interact with Clinical Data Scientist at study level for deliverables.Serve as a technical resource to the study teams for data visualization and reporting tools and provide technical expertise and business process support in technology systems.Ensure operational excellence in collaboration with partners for application of standards, data acquisition, proactive data review and data integrity and overall data management activities.Partner with Research/Business Units and any external DM service provider to deliver high quality data management for all studies as assigned.Perform central monitoring activities including review system outputs, propose suggestions for signal and action management, and follow up with study team for the action resolutions.Plan and execute communication plans and methods for engaging customer populations.QualificationsMust-HaveBachelor s Degree5 years’ experienceExperience within the pharmaceutical industry or in a health information management roleWorking knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol reviewWorking knowledge of clinical research, Food and Drug Administration