職位描述：

職責描述：

1.負責疼痛科日常診療工作；

2.根據患者需求和個體情況，能提供專業性建議和治療方案，并能從事疼痛科相關手術診療工作；

3.負責根據治療方案，確保治療質量；

職位要求：

1、臨床專業大專或本科學歷，具有中級以上職稱；

2、具有疼痛科臨床工作經驗；

3、熟練疼痛科常見病的診斷及治療；

4、具有良好的職業道德與和高度的責任心。

篇2:疼痛科醫師崗位職責任職要求

疼痛科醫師崗位職責

職責描述:

1、負責疼痛科日常診療工作;

2、根據患者需求和個體情況,向患者提供專業性建議和治療方案,為患者提供專業咨詢;

3、負責根據治療方案,實施皮膚治療,確保治療質量。

任職要求:

1、中醫、臨床等相關醫學專業畢業,本科學歷;

2、善于運用中西醫結合的方法,治療各種勁肩腰腿痛等疾病;

3、持執業醫師資質證書,可變更注冊;具有副主任醫師及以上職稱;

4、有中醫、骨科、康復、理療等臨床診療5年以上工作經驗。

疼痛科醫師崗位

篇3:MA醫學顧問疼痛，骨科，風濕科，神經內科，麻醉科工作職責與職位要求

職位描述：

職責描述：

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