職位描述：

職責(zé)描述：

Toadviseandmanagemedicalrelatedactivitiesinalloperationsofcompanywithmedicalexpertiseandcompanypolicies,withtheobjectiveofensuringthescientificvalidityandtheethicsofoperations.

1.EnhancelocaldatagenerationandProductlife-cyclemanagementfrommedicalperspectivetomaximizeproduct’svalueandlongtermdevelopment

?Evaluatenewproducts,newindications,newresearchprograms,newbusinesspotentialsofdefinedtherapeuticareasfrommedicalperspectivetosupportnewproductintroductionandlineextension

?Alignwithcrossfunctionteamincludingmarketing,CCOteam,globalteametc,developpostmarketingresearchstrategybasedonRegistration/Marketneeds

?ProvidephaseIVstudydirectionanddevelopkeyelements

?DesignandmanagelocalNon-interventionalStudy(NIS)studyasaclinician.

?Developmedicalstrategyandimplementittosupportproductdevelopment

?Developpublicationplanandimplementit

?EvaluateandreviewInvestigatorInitiateresearchproposaltoensureitsscientificstandardandstrategyfit

2.Asakeypartnertoprovidemedicalinputonbusinessdecisionmaking

?Co-developproductstrategy,positioning,keymessagewithMarketingteam

?Providemedicalsupport(topicdesign,KOLcommunicationetc.)onkeymarketingactivities

?Providebroadanddeepmedicalinsight/summarydocumentofthedefinedtherapeuticareatobusinesspartnerstodealwithkeyproductissuessuchasbidding,RDL,newinitiativesetc.

?ReviewandapproveLocalStandardResponseLettertoHCPs

3.Developsaleforce’smedicalcapabilitythroughtrainingprogramdesign,LectureDeliveryandperiodicmedicalknowledgeupdateindifferentsettingsthroughvariouschannel

?AtPhaseIsalestraining

?AtNationalsalesconference

?Fieldvisit

?Specialsalesforceprogram

?Givelecturesorupdatestootherstakeholderstoincreasetheirdiseaseandproductknowledge

4.SupportDrugRegistrationActivities

?Timelyreviewandapprovaloflocalproductlabeling(LPD)

?DevelopmedicaljustificationdocumenttosupportLPDrelatedqueriesfromgovernment

?Providemedicalinputinfeasibilityevaluationofstudiesforglobaltrials

?Provideofficialinputonstudysiteselectionfromtherapeuticprospective

?Provideinputtoregistrationprotocolsynopsisandstudyreportasnecessary

5.AcademiccommunicationtoenhancethedeliveryofnewconceptandPfizerproductskeymessagetokeyinfluencersandstakeholders,andEstablishCooperationandpartnershipwithmedicalassociationtopromotemedicaladvancement.

?SetupnationallevelKOLdatabase,andkeepmedicalcommunicationwiththroughvariousapproaches

?DesigneducationalprogramsfortopKOLsandimplementthem

?SupportonChinatreatmentguidelinedevelopment,scientificinterpretationandpromotion

?Publishorfacilitatepublicationofmedicalpaperinprofessionaljournals

?Cooperationwithlocalmedicalsocietiestoconductmedicalprograms/conferencetofacilitatenewconceptandstateofartmedicalprogress’introductiontoChina

6.Inordertomaintaincompany’simageandprotectpatient’swelfare,MAactasacoremembertoworkwithcrossfunctionteamoncrisismanagement.

?Performmedicalevaluation,explanationontheevent;

?Developmedicaljustificationorrespondingdocument.

?Providemedicalexpertopiniononcompanyrespondingstrategy

?Reviewandapproveallexternalcommunicationdocumentstomakesurealldeliveredmessagearemedicallypreciseandconsistent

?Communicatewithexternalcustomersdirectlyformedicalissuesasnecessary

7.Providemedicalexpertopinioninsafetyeventsmanagementtoavoidnegativeimpact.

?ProvideprofessionalmedicalconsultationtoSafetyOfficertosolvePfizerproducts’safetyquery

?Iftakeclinicianrole:providetheclinicalsafetyoversightincludingperforminganddocumentingregularreviewofindividualsubjectsafetydataandperformingreviewofcumulativesafetydatawiththesafetyrisklead(asdelegatedbytheclinicallead).

?Iftakeclinicalleadrole:consistentwithSafetyReviewPlan(SRP),performsanddocumentsregularreviewofindividualsubjectsafetydata,andperformsreviewofcumulativesafetydatawiththesafetyrisklead.Asappropriate,theclinicalleadmaydelegatetheseresponsibilitiestothestudyclinicianidentifiedintheSRP.ThespecificcomponentsofsafetydatareviewaredetailedintheSafetyDataReviewGuide–forCliniciansandinSAF09SOP.Forallstudies,clinicalsafetyreviewshouldbeperformedinconsultationwithadesignatedmedicalmonitorifneitherclinicalleadnorcliniciansaremedicallyqualified.

8.Ensurecompany’smedicalcompliance.

?Actasthesolereviewertoensureeducationalgrantswithinmedicalcompliance

?Reviewandapprovepromotionalmaterialsandactivitiestoensuretheirscientificstandardandmedicalcompliancewithexternalandinternalrequirements

篇2:人民醫(yī)院麻醉科醫(yī)師職責(zé)

市人民醫(yī)院麻醉科醫(yī)師職責(zé)

一、在科主任領(lǐng)導(dǎo)下和主任醫(yī)師指導(dǎo)下,負(fù)責(zé)本科日常麻醉教學(xué)科研的具體工作。

二、麻醉前檢查手術(shù)病員,必要時(shí)參加術(shù)前討論與醫(yī)師共同研究確定麻醉方法和麻醉前用藥,做好麻醉前的藥品器械準(zhǔn)備。

三、麻醉中,經(jīng)常檢查輸血、輸液及用藥情況,密切觀察病情,認(rèn)真填寫麻醉記錄單。如出現(xiàn)異常變化及時(shí)與術(shù)者聯(lián)系,共同研究,妥善處理,并報(bào)告上級(jí)醫(yī)師。

四、手術(shù)后對(duì)危重和全麻病員親自護(hù)送(包括術(shù)者),并向病房護(hù)士交待病情及術(shù)后注意事項(xiàng)。

五、手術(shù)后進(jìn)行隨訪,將有關(guān)情況記入麻醉記錄單并做出麻醉小結(jié)。

六、遇疑難病例不能單獨(dú)處理時(shí),應(yīng)及時(shí)報(bào)告上級(jí)醫(yī)師。

七、嚴(yán)格執(zhí)行各項(xiàng)規(guī)章制度和技術(shù)操作規(guī)程,嚴(yán)防差錯(cuò)事故。

八、積極開展麻醉的研究,參加科研及教學(xué),做好進(jìn)修、實(shí)習(xí)人員的培訓(xùn)。

九、協(xié)助各科搶救危重病員。

篇3:人民醫(yī)院麻醉科科主任職責(zé)

市人民醫(yī)院麻醉科科主任職責(zé)

一、在院長(zhǎng)及分管副院長(zhǎng)領(lǐng)導(dǎo)下,負(fù)責(zé)全科的醫(yī)療、教學(xué)、科研、行政管理等工作。

二、制定本科工作計(jì)劃,組織實(shí)施,經(jīng)常督促檢查,按期總結(jié)匯報(bào)。

三、根據(jù)本科任務(wù)和人員情況進(jìn)行科學(xué)分工,密切配合手術(shù)和對(duì)危重病人進(jìn)行搶救工作。

四、領(lǐng)導(dǎo)麻醉師做好麻醉工作,參加疑難病例術(shù)前討論,對(duì)手術(shù)準(zhǔn)備和麻醉選擇提出意見,必要時(shí)親自參加操作。

五、組織本科人員的業(yè)務(wù)訓(xùn)練和技術(shù)考核,對(duì)本科人員晉升、獎(jiǎng)懲提出具體意見。

六、領(lǐng)導(dǎo)本科人員認(rèn)真執(zhí)行各項(xiàng)規(guī)章制度和技術(shù)操作規(guī)程,嚴(yán)防差錯(cuò)事故。

七、組織并擔(dān)任教學(xué),安排進(jìn)修、實(shí)習(xí)人員的培訓(xùn),開展麻醉的研究工作。搞好資料積累完成科研任務(wù)。

八、確定本科人員輪換、值班會(huì)診、出診等事宜與手術(shù)室密切配合共同做好科室工作。

九、審簽本科藥材的請(qǐng)領(lǐng)和報(bào)銷,檢查使用與保管情況。

副主任協(xié)助主任負(fù)責(zé)相應(yīng)的工作,主任不在時(shí)履行主任職責(zé)。