「Pharmacist」找工作職缺-2022年8月|104人力銀行
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... Sales Specialist【台灣大昌華嘉股份有限公司】。
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8/29
【醫療保健事業單位HealthcareBusinessUnit】PharMD-數位業務專員(南區)Specialist,DigitalSales
台灣大昌華嘉股份有限公司
其他醫療保健服務業
高雄市三民區
3年以上
大學Jobsummary:
DigitalSalesSpecialistisresponsibleforapplying,testingnewdigitalsalestechniques(platformsortools)andachievingsalestargetsinanassignedterritorythrougheffectiveexecutionofthesalesstrategyandproactive(outbound)contact,overallterritory/accountmanagement,andvisittotheassignedcustomer
Generalresponsibilities:
1.Consistentlyachievebusinessobjectives&salestargetsestablishedbyleadershiputilizingdefineddigitalplatformsandtools,proactive(outboundviaphysicalvisits,tele-orsocialmediaplatform)contact,overallterritorymanagement,andteamcollaboration.
2.Efficientlymanageterritorythroughcustomer/accountplanningfordigitalplatform/tools,andengagementwithkeystakeholderswithincustomersincludingendusersofdigitalplatform/tools,KOL(keyopinionleaders)andprocurement.
3.Maintainaleveloftechnicalandapplicationcompetenceandutilizethisknowledgeinamannerwhichwillenablehim/hertoaddvalueandpromoteCX(customerexperience)improvement.Maintaineffectiveandprofessionalcommunicationwithcustomers
4.Scheduleandexecutecampaignsandpromotionswithinthedefinedterritory.Assistinginthesalesprocessthroughdataanalysis,collectingrelevantdata,verifyingdataintegrityofcustomersdata,translaterawdataintoactionableMA(MarketingAutomation)bysellinginsights,andtofeedbacktoCHC&PharmaSalesTeamforpotentialunmanagedaccountsdevelopment.
5.Provideinsightsforthecustomerprofiling&segmentationofTierAcustomersforamoreaccurateexecutionofassignedDigitalPlatformswithCHC&PharmaSalesTeam
待遇面議外商公司員工1500人
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7/13
(Sr.)PatientSafetySpeciaist
台灣諾華股份有限公司
其他醫療保健服務業
台北市中山區
5年以上
大學1.Managecollection,processing,documentation,reportingandfollow-upofalladverseeventreportsforallNovartisproductsfromclinicaltrials,non-interventionalstudies,PatientOri-entedPrograms,literature,SpontaneousReports,etc.Transcribe,translateandenterdataofalldatafromsourcedocumentsintosafetysystemsaccuratelyandconsistentlywithempha-sisontimelinessandquality.
2.Managereporting/submission/distributionofsafetyreports/updates/information(e.g.SAE,SR,IN/SUSAR,PSUR,BiannualSUSARListing,DSUR)toLocalHealthAuthorities(LHA)and/orclinicaloperationsincooperationwithotherCountryOrganizationDepartments.
3.Workwithotherlocal/globalPatientSafetyassociatestoensureaccurateevaluationofsafetydata.
4.InteractandexchangerelevantsafetyinformationwithLHA,PatientSafetyassociates,otherfunctionalgroupsandthirdpartycontractor,ifapplicable.
5.SurveyandmonitornationalpharmacovigilanceregulationsandprovideupdatetoglobalPatientSafetyorganization.
6.Develop,updateandimplementlocalprocedurestoensurecompliancewithPatientSafetyglobalproceduresandnationalrequirements.
7.Input,reviewandapprovalofprogramproposalsforlanguage,contentandestablishmentofnecessarycontrolsoncollectionandreportingofadverseeventinformation.
8.Performreconciliationwithotherdepartments(e.g.MedicalInformation,QualityAssuranceandthirdpartycontractor,ifapplicable)forpotentialAEsresultingfrommedicalinquiries,qualityrelatedcomplaintsandothersources.
9.ManagementandmaintenanceofallrelevantPatientSafetydatabases.
10.Ensurethatrelevantlocalliteraturearticlesarescreenedasappropriate.
11.PrepareandsubmitKPIreportsoncomplianceinatimelymannerincludingidentificationofrootcause(s)forlatereportingtoLHA,developmentandimplementationofcorrectiveaction(s)asneeded.
12.DevelopandupdatetrainingmaterialsforpharmacovigilanceandensuretrainingofCountryOrganizationassociatesonrelevantPatientSafetyproceduresforAEreporting,includingfieldforceandthirdpartycontractor,ifapplicable.
13.Ensuresupportforandclose-outofaudits,correctiveactionplan,investigationandHealthAuthorityinspections.
14.Ensuretrainingandoversightofstaff,asapplicable.
15.ManageandmaintainefficientPatientSafetyfilingandarchivesystem.
16.ReviewofallPhaseIVClinicalTrialandNISprotocolssafetysectionsandifaContractRe-searchOrganization(CRO)isconductingthetrial,reviewthecontract(SSW),traintheCROassociatesresponsiblefromthetrial
17.DrivesthelocalexecutionoftheRiskManagementPlans(RMP)forallNovartisgroupprod-uctsin(insertCountryOrganization):
•EnsurestrainingonRMPprinciplesandRMPproductspecificsofCountryOrganizationstaff(incl.Sales/Marketingstaff)involvedintheimplementationoftheRMP
•SupportstheDrugSafetyResponsibleinthetimelyandcompliantexecutionlocallyofthePharmacovigilanceactivitiesdefinedintheRMP
•LiaiseswiththeotherdepartmentsintheCountryOrganizationsuchasClinicalRe-searchOperations,Medical,RegulatoryAffairsorSales/MarketingtoensurealignmentofalllocalfunctionsinsupportoftheRMP
•LiaiseswithSales/Marketingtoensureimplementationofeducationalmaterials
18.LiaiseswithLocalRegulatoryAffairstoensuretrackingofstatusoftheRMPcommitmentsimplementedlocally
19.Andotheragreedtasksassignedbymanager待遇面議外商公司員工600人
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8/29
AsiaHubLabelingAssociate約聘亞太產品仿單規劃整合專員(派駐輝瑞大藥廠)
就業情報資訊股份有限公司
人力仲介代徵
台北市信義區
1年以上
大學1.Tosupportinuploadinglabelcontentsintodatabasewithquality
2.TosupportHLMwithotheroperationalactivities,e.g.,datamaintenance
3.Tocompletesimpleadhoclabelupdates
4.Tocompleteproof-readingofthelabeltext待遇面議員工450人距捷運象山站340公尺
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應徵0~5人應徵
8/24
法規事務人員
安成國際藥業股份有限公司
藥品製造業
台北市內湖區
3年以上
大學1.TopreparetimelyoriginalANDAs,amendments,andsupplements,includinginterfacingwithotherdepartmentstoobtainthenecessarycomponentsanddraftsreportsandnarrativecomponents
2.TocontactbetweenQAandRAfordocumentchangecontrol
3.Toassistinapplicationtootherregulatoryauthority
4.Toassistindeficiencyletterresponse
5.Othertemporarymattersassignedbysupervisor待遇面議員工288人
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8/05
253523Sr.RegulatorySpecialist/RegulatoryExpert資深法規專員
德商默克在台集團_台灣默克股份有限公司
生化科技研發業
台北市內湖區
3年以上
大學JobObjective:
ThispositionwilleffectivelydriveandmanageregulatorystrategyforLSproductsandservices,coordinateandengageinregulatorytasksforOurCompanyLifeSciencebusinessinTaiwan,includingproductregistrations,supportingbusinessregulatoryneedsandcustomerrequests.Facilitateandmaintainexcellentworkingrelationshipwithregulatoryauthoritiesandcustomers.SeekingadviceoninterpretationoflocalGovernmentalregulationsandrequirements,andconductregulatorysurveillanceforOurCompanyLifeScienceproductscomplianceinconsideringtheirintendeduseontheirrespectivemarkets.
JobResponsibilities:
ThisjobwillbebasedinTaipeiwithflexibility.
.Developappropriateregulatorypathwaytomarketandsupportpost-marketactivitiesforOurCompanyLifeScienceproductsandservicesinTaiwanasregulatoryrepresentative,coveringtheareasofdrugreferencestandard,APIs,foodadditives,dietaryingredients,andmedicaldevices/IVDs/CTRFD(TheControlledTelecommunicationsRadio-FrequencyDevices)etc.
.Proactivelyplanandengageinregistration/notification/listingactivitiesinTaiwan.Ensurethecorrectnessandtimelinessoftheseactivities,interimfollow-upchangemanagementandfinaloutcome.Ensuretracking,maintenanceandreportingofregistration/notification/listingstatus.
.Workcloselywithbusinesspartnerstoensurethattheiroperationsandprocessescomplywiththerelevantlegalregulations.
.Monitorchangeswithinrelevantregulatoryandcomplianceenvironment,influenceandshapefutureguidance,regulationsandpolicy.
.Provideregulatoryguidanceinriskassessment,identifyregulatoryimpacttoourcompanyandprovideregulatoryrecommendationstomitigatepotentialrisk.
.IncreasefocusonbuildingandstrengtheningrelationshipwithTaiwanregulatoryauthoritiestomitigatecompliancerisksandsafeguardourcompanyinterest.
.BuildandmaintainexcellentrelationshipwithTaiwanregulatoryauthoritieswitheffectivewrittenandverbalcommunication.
.TakeactiveroletorepresentcompanyindelicateorriskpotentialmatterswithTaiwanregulatoryauthoritiesandindustryassociations.
.Provideregulatorysupporttomarketing,salesandcustomersviaconsultation,seminarsandtrainingevents.待遇面議外商公司員工235人
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應徵11~30人應徵
8/26
QASpecialist(DrugProdcut)
潤雅生技股份有限公司
其他相關製造業
新竹縣竹北市
3年以上
大學1.GMPdocumentsreviewandapproval.
2.Conductsupplierqualificationprogramforvendors.
3.Conductin-process,rawmaterialandstabilitysampling.
4.AssistQAManagementinmanagingdeviation,investigation,CAPAsystems,stabilityprogramandQualitySystemstocomplywithapplicableregulatoryrequirements.
5.ReviewandcreateQA-relatedSOPs.
6.MiscellaneoustasksassignedbyManagement.待遇面議員工50人
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8/09
西藥部-MedicalScienceLiaison(腎臟科)
荷商葛蘭素史克藥廠股份有限公司台灣分公司
藥品製造業
台北市中正區
2年以上
大學KeyAccountabilities/Responsibilities:
1.Bethescientificexpertforaparticularmedicineorgroupofmedicinesina
therapyareaintheassignedgeography.
2.Maintainadetailedunderstandingofthetherapyareaandadeepappreciationof
thescienceandevidenceforGSKmedicinesandothernon-GSKtreatmentoptions
inthetherapyarea.
3.Actastheinterfacebetweentheprofessionalhealthcarecommunityandthe
internalGSKmedicalteamanditsaffiliatesprovidingvalue-addedinsightsand
feedbackfromthecommunitydesignedtoimprovemedical,commercialanddrug
developmentplanningandserviceprovision.
4.Bepreparedtorespondtoanyenquiriesfromlocalhealthauthorities/tenderswith
regardtoGSKvaccinesafety/efficacy/effectivenesstoensurecoveredvacineesare
benefited,andworkcloselywithtenderandGAteamsforthecommunicationwith
HA/tenders/policymakers.
5.FullyunderstandandalwaysmeettherequirementsintheGSKStandardsfor
ScientificEngagement(POL-GSK-002andSTD-GSK-002),ExternalInteractionsby
MedicalandR&DStaff(STD-GSKF-415)and,whererelevanttopromotional
activities,theGSKCodeofPracticeforPromotionandCustomerInteractions(STD-
GSK-401).
6.Fullyunderstandandcomplywithlocalcodesofpractice,guidelinesandlawsto
ensurethestrictestrequirementsaremetparticularlywithrespecttodeliveryof
promotionalversesnon-promotionalinformation.
7.Respondcompliantlytounsolicitedinformationrequestsfromhealthcare
professionalsandassociatedindividualsregardinglicensedorun-licensedGSK
medicinesandindications;ensureallmedicalinformationresponsesarefactual,
fairandbalanced,scientificallyrigorousandstrictlycomplywithlocalregulations.
8.Disseminateimportantsafetyinformationtothehealthcareprofessionasdirected
bytheMedicalAffairsorResearchandDevelopmentteamsortheDearHealthcare
ProviderLetter(DHPL)process.
9.Assistthemedicalteamintheidentificationofexternalexpertswithinthetherapy
areaandgeography.
10.SupportGSKstudyteamswiththeprovisionofscientificeducationandenquiry
managementfrominvestigatorsandstaffengagedinGSK-supportedclinical
trialse.g.Investigator-SponsoredStudies(ISS).
11.ProvidescientificeducationtrainingforbusinesspartnerssuchastheMedical
Representatives.
待遇面議外商公司員工200人距捷運台北車站270公尺
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8/24
藥劑科-藥師【年薪81~84萬(特殊津貼另計),單人宿舍,客運每20分一班,至台北車程約1小時】
醫療財團法人羅許基金會羅東博愛醫院
醫院
宜蘭縣羅東鎮
經歷不拘
大學分鐘路程,宜蘭空氣清新、生活居住環境適宜,物價低,可享受慢活樂趣。
★藥劑科簡介★
http://ehr.pohai.org.tw/index.php/advanced-stuff-2/pharmacist-recruit年薪810,000~840,000元員工1700人
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8/09
西藥部-MedicalContentSupervisor
荷商葛蘭素史克藥廠股份有限公司台灣分公司
藥品製造業
台北市中正區
2年以上
大學EssentialJobResponsibilities:
1.CopyApproval
➢LeadsandactsasLOCmedicalsignatoryrelatedtopromotionalandnon-promotionalmaterialrequiringcopyapprovalforTaiwan
➢Abilitytocheckstranslationaccuracyofmaterials,medicalreviewandlocalization.
➢Abletocarryoutdaytodayactivitieseffectivelywithoutsupervision.
2.Scientific&ProductExpertise
➢DemonstrateknowledgeofconceptsofscientificandclinicaldatainoneormoretherapeuticareasandrelatedGSKproducts,includingtherelatedclinicalstudiesandtheirdesiredpositioninginthemarketforsuchproducts.
➢Understandstherisk/benefitprofilesofGSKproducts.
➢UnderstandsTA/productstrategyforkeyproductsinthepromogrid.
➢PartnerwithContentManagertoreviewglobalintegratedcampaigns,identifygapsandcoordinategenerationofcontenttoaddressgaps.
➢Understandsthepopulationsandendpointsselectedandtheclaimsthey(areintendedto)support.
➢Demonstratestrongunderstandingoftheinterpretationofclinicalstudiesresults.
3.MedicalGovernance
➢MedicalreviewandapprovalofLOCmaterialsinaccordancewithlocalregulations.
➢WorkwithCommercialtoensurethatmaterialsusedinlocalmarketsareinlinewithGSKrequirementsandtotherequiredstandard.
➢Ensuresfullcompliancewithgovernanceprincipleswhilstseekingappropriatebusinesssolutions,atLOClevel.
➢Demonstratesahighlevelofpersonalaccountabilityandintegrity.
➢SupportandcoordinatewithLOCMGL(medicalgovernancelead)forMMmonitoringandCAPATracking.
➢Appliesgoodjudgment:seekssolutionsthatmeetbusinessneedswhilstremainingcompliantwithGSKValuesandprinciples.
4.OperationalExcellence
➢Demonstratesahighlevelofpersonalaccountabilityandintegrity.
➢PartnerwithCommercialtoapplymetricseffectivelytoensuredeliveryandtocommunicateprogresstostakeholders.
➢Abletoidentifyprocessimprovementopportunitiestobusinessproblems.
5.Effectivecommunication
➢Effectiveinterpersonalrelationshipwithstakeholders.
➢Effectivenetworkingandcollaborationskillstoachievebusinessresults.
6.BusinessSkills
➢Strongbusinessmindset.
➢Builtcorporatebehavioraddingvaluetothebusiness.
7.PeopleManagement
➢Trainandcoachothersoncopyapprovalprocessforoneormoretherapeuticareas(tosupportyourbusinessstakeholdercounterpart)
待遇面議外商公司員工200人距捷運台北車站270公尺
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應徵6~10人應徵
8/29
MedicalAffairsSpecialist
安沛國際有限公司
藥品製造業
台北市大安區
2年以上
大學PrimaryObjectives:
Pharmacovigilance(PV)
1. PVrequirementsperGrouppolicy(monthlyreport)
2. PVobligationperlocalregulations(safetyreporting)
3. PV-QMSdocumentsestablishment
4. PVtrainingandSDEAmanagement
5. Collection,follow-upandforwardingofspontaneous,literature,solicited,post-marketingAEcasesMedicalInformationfunction
QualityAssurance(QA)
1. Batchreleaseataffiliatelevel
2. ManagementofPQCreporting,sampleretrievinganddeliveringtositeforinvestigation
3. ManagementofAGIinvestigationreportandcommunicatetocustomersand/orHealthAuthority
MedicalInformation(MI)
1. ManagementofMedicalInquiryregistry,reportingandtracking
2. PromotionalMaterialreview
RegulatoryAffairs(RA)
1. Licenserenewal,leafletupdateandminorCMCvariation
2. OtherassignedRAactivities
JobResponsibilities:
ResponsibilitiesforPV:
1. MaintainingtheoverviewofthelocalPharmacovigilancesystem
2. HavingfullunderstandingofthesafetyprofilesofAspengroupproducts,includinganyemergingsafetyconcerns,riskminimisationmeasuresandconditionsorobligationsrelatedtotheirsafetyuse
3. ActasapointofcontactforthelocalregulatoryauthoritiesandAPTLPV
4. EnsurescompliancewiththeAGIpoliciesaswellaslocalPVregulations
5. ICSRprocessingandCIOMSHealthAuthoritysubmission
6. EstablishandmaintainlocalPVqualitysystem
7. Supportslocalsafetysurveillanceactivitiesbylookingatandmonitoringeventfrequencies/severityatlocallevel
ResponsibilitiesforQA:
1. Batchreleaseataffiliatelevel
2. ManagementofPQCreporting,sampleretrievinganddeliveringtositeforinvestigation
3. ManagementofAGIinvestigationreportandcommunicatetocustomersand/orHealthAuthority
ResponsibilitiesforMI:
1. Medicalinformationenquiryhandling,includingregistry,answering,followup,closeout
2. Promotionalmaterialmanagement,includingreview,documentationandupload
3. Ensuringaprocessisinplacetoperformtestingonceayearforallchannelswherethereisapotentialtoreceivemedicalinformationenquiries
4. Ensuringaprovisionisinplacetoreceivemedicalinformationenquiriesduringoutofofficehours
5. Productinformationmanagement
ResponsibilitiesforRegulatoryAffairs(RA):
1. Licenserenewal,leafletupdateandminorCMCvariation
2. OtherassignedRAactivities
Otherassignedactivities,supportingtasksorsysteminformationupdate待遇面議距捷運六張犁站440公尺
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8/01
QualityManager品保主管
台灣禮藍動保股份有限公司
綜合商品批發代理業
台北市松山區
3年以上
大學PositionDescription:
AsthecentralqualitycontactfortheElancoMarketingAffiliateorganization,theQUALITYMANAGERadvises,decidesreports,consultsandescalatesqualitymattersrelatingtoElancoproductsdistributedinTaiwanandHongKong,totheappropriateaffiliatemanagement,DirectorofQualityGreaterChina,RegionalQualityLeaderorCorporatemanagementwhenneeded.
COREJOBTASKS
• Beresponsibleforproductqualityrelatedmatters,escalateanylocalproductqualityrelatedissuetoDirectorofQualityGreaterChina,RegionalQualityLeaderandtheaffiliatemanagement,andcollaborateinanylocalactiontobetakenasaresultofthat(i.e.recall,counterfeitetc.)
• ImplementandmonitorproductqualitysystemsandQualityManualintheMarketingaffiliate.
• Assistaffiliatemanagement,DirectorofQualityGreaterChina,RegionalQualityLeaderinassuringthatalloperationsoftheaffiliatecomplywiththeAffiliateQualityManualandotherapplicablecompanyqualitystandards,GQPandlocalregulations.
• ExecutetheassessmentplanforGMPServiceProviders.
• CreateandreviseQualityagreementscoveringaffiliateprocessesforGMPserviceproviders.
• Demonstratecontinuousimprovementandminimizeriskbyaroutineself-assessment,correctiveandpreventativeactions(CAPA),anduseofaQualityPlan.
SPECIFICAREASOFACCOUNTABILITY/RESPONSIBILITY
1. QualityManagement
• EnsureaffiliatecompliancewithGoodManufacturingPractices(cGMP),GoodWarehousingpractices,GQPandgoodLocaltestingpracticesforfinishedproducts.Alsoensureaffiliatecompliancewithallrelevantlocalregulations.
• Conductquarterlyandannuallytrends(events,complaints,approvals).
• Ensureanannualmanagementreviewisconducted.
• EnsureNotificationtoManagementwithinonedayofidentification.
• Halt,holdorquarantineproductstatusasrequired.
2. QualitySystems
3.BatchRelease
4.ChangeandEventManagement
5.Documentation
Maintainlocalprocedureswhichreflectlocalregulations(whererequired)andcorrespondingglobalqualitystandards.
Createorreviewrelevantqualityrelateddocuments,
6.PersonnelQualifications
MaintainajobdescriptionandCVthatdescribesthequalitydutiesandreviewiteverytwoyears.
7. Review,andapproveGMP,GQPtrainingmaterialsordocumentsgeneratedbythelocalaffiliateandensuretrainingrecordsaredocumented
8.QualityPlan
9.AuditingandInspections
• Conductself-assessmentsofqualitysystemsatleastannually,tomaintainastateofinspectionreadinessattheaffiliate.
• AssessGMPsuppliersandserviceproviderswhereapplicableaccordingtoanapprovedplan.
• Facilitateandco-ordinateRegulatoryAgencyinspections,EGQCAauditsoftheaffiliateandserviceproviders.Supporttheaffiliatewiththeauditreadinessplan.TakedailynotesandreportthedailyauditactivitiestotheaffiliateLeadTeam.
• PreparewrittenresponsestoEGQCAauditsbyconsultingwithDirectorofQualityGreaterChina,RegionalQualityLeader.PreparewrittenresponsestoregulatoryagencyinspectionsbyconsultingwithDirectorofQualityGreaterChina,RegionalQualityLeader,GlobalSeniorQualityDirectorandDirectorofEGQCA.Ensuretimelyresponsesandexecutionofactionsbytargetduedates.
• ReviewandconsultonallnewbusinessdealsthatrequirequalityoperationswithDirectorofQualityGreaterChina,andRegionalQualityLeader
• CreateandreviewQualityAgreementsforco-promotions,distribution,branddivestmentsandnon-trademarksupplyagreements
10.RegulatoryInteractionswithGovernmentAgencies
11.AdverseEventsandProductComplaints
12Recalls
13.HealthHazardEvaluation(HHE)
14.ComputerSystems
15.MaterialsManagement
16.DistributionofFinishedProducts
17.PackagingandLabeling
18. EnvironmentHealthandSafely
月薪50,000元以上員工48人遠端工作
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8/19
臨床試驗營運部_臨床研究專員(CRA)[台北]
友華生技醫藥股份有限公司
藥品製造業
台北市北投區
5年以上
大學*PositionSummary:
Colleagueinthispositionwillberesponsiblefordirectlymonitoringclinicaltrialsassignedbyhis/hersupervisororexecutivemanager.HeorshemayalsoplaytheroleofLeadCRAundersupervisorsupportingandDepartmentalCoordinatorrolesfortheassignedtasks.
*KeyResponsibilities:
1.ClinicalTrialApplication.
2.PrepareandcollectrequireddocumentationsforIRB/IECandregulatoryauthorities’submissionactivities.
3.CoordinateandcommunicatewithIRB/IECandregulatoryauthoritiesforproperreplytotheirreviewcomments.
4.Guideincomingstudyteammembertofamiliarthesubmissionprocessoranyprojectspecificrequirement.
*SiteIdentification&Qualification:
Assistclinicalprojectteaminevaluatingpreviouslyusedsitesinordertocollectarealisticassessmentofasite’squalificationandrecruitmentcapabilityandtoidentifynewsites.待遇面議上市上櫃員工950人
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應徵0~5人應徵
8/09
西藥部-MedicalScienceLiaison(呼吸道specialtycare)
荷商葛蘭素史克藥廠股份有限公司台灣分公司
藥品製造業
台北市中正區
2年以上
大學KeyAccountabilities/Responsibilities:
1.Bethescientificexpertforaparticularmedicineorgroupofmedicinesina
therapyareaintheassignedgeography.
2.Maintainadetailedunderstandingofthetherapyareaandadeepappreciationof
thescienceandevidenceforGSKmedicinesandothernon-GSKtreatmentoptions
inthetherapyarea.
3.Actastheinterfacebetweentheprofessionalhealthcarecommunityandthe
internalGSKmedicalteamanditsaffiliatesprovidingvalue-addedinsightsand
feedbackfromthecommunitydesignedtoimprovemedical,commercialanddrug
developmentplanningandserviceprovision.
4.Bepreparedtorespondtoanyenquiriesfromlocalhealthauthorities/tenderswith
regardtoGSKvaccinesafety/efficacy/effectivenesstoensurecoveredvacineesare
benefited,andworkcloselywithtenderandGAteamsforthecommunicationwith
HA/tenders/policymakers.
5.FullyunderstandandalwaysmeettherequirementsintheGSKStandardsfor
ScientificEngagement(POL-GSK-002andSTD-GSK-002),ExternalInteractionsby
MedicalandR&DStaff(STD-GSKF-415)and,whererelevanttopromotional
activities,theGSKCodeofPracticeforPromotionandCustomerInteractions(STD-
GSK-401).
6.Fullyunderstandandcomplywithlocalcodesofpractice,guidelinesandlawsto
ensurethestrictestrequirementsaremetparticularlywithrespecttodeliveryof
promotionalversesnon-promotionalinformation.
7.Respondcompliantlytounsolicitedinformationrequestsfromhealthcare
professionalsandassociatedindividualsregardinglicensedorun-licensedGSK
medicinesandindications;ensureallmedicalinformationresponsesarefactual,
fairandbalanced,scientificallyrigorousandstrictlycomplywithlocalregulations.
8.Disseminateimportantsafetyinformationtothehealthcareprofessionasdirected
bytheMedicalAffairsorResearchandDevelopmentteamsortheDearHealthcare
ProviderLetter(DHPL)process.
9.Assistthemedicalteamintheidentificationofexternalexpertswithinthetherapy
areaandgeography.
10.SupportGSKstudyteamswiththeprovisionofscientificeducationandenquiry
managementfrominvestigatorsandstaffengagedinGSK-supportedclinical
trialse.g.Investigator-SponsoredStudies(ISS).
11.ProvidescientificeducationtrainingforbusinesspartnerssuchastheMedical
Representatives.
待遇面議外商公司員工200人距捷運台北車站270公尺
不想看到這個公司
不想看到這個產業
儲存
應徵6~10人應徵
8/24
Analyst/AssociateConsultant,RWE/HEOR
IQVIA_艾昆緯藥品資訊股份有限公司
其他醫療保健服務業
台北市松山區
經歷不拘
大學PositionPurpose:
Provideshighquality,on-timeinputtoclientprojectsinthelifesciencesfield.Assignmentstypicallyrequireanalysisandproblemsolvingwithinanestablishedframework.
PrincipalAccountabilities:
*Underdirectsupervision,assistswiththereviewandanalysisofclientrequirementsorproblemsandassistsinthedevelopmentofclientsolutions.
*Assistsinthedevelopmentofdetaileddocumentationandspecifications.
*Underclosesupervision,performsquantitativeorqualitativeanalysestoassistintheidentificationofclientissuesandthedevelopmentofclientspecificsolutions.
*Assistsinthedesignandstructureofpresentationsthatareappropriatetothecharacteristicsorneedsoftheaudience.
*Proactivelydevelopsabasicknowledgeofconsultingmethodologiesandthelifesciencesmarketthroughthedeliveryofconsultingengagementsandparticipationinformalandinformallearningopportunities.
*EngagementbasedresponsibilitiesareassignedandcloselymanagedbyConsultants,SeniorConsultants,EngagementManagersorPrincipals.
JobDescriptions:
*SupportclienttodevelopPRA(Pricing,Reimbursement&Access)strategy
*HelptopreparePricingandReimbursementdossier
*Understandanduselocalclinicaldata/literature/publicdomaininformation/face-to-faceinterviewwithclinicalexpertstoaccessbudgetimpactandcosteffectivenessmodel
*Cross-functionalcoordination,cooperationandcommunication
*Developpayervaluemessagebasedonlocalunmetmedicalneeds
*Familiarwithcurrentnationalhealthcareenvironment,policyandfuturetrend待遇面議外商公司遠端工作距捷運中山國中站470公尺
不想看到這個公司
不想看到這個產業
儲存
應徵0~5人應徵
8/05
西藥部-Sr.MedicalScienceLiaison(Vaccine)
荷商葛蘭素史克藥廠股份有限公司台灣分公司
藥品製造業
台北市中正區
2年以上
大學KeyAccountabilities/Responsibilities:
1.Bethescientificexpertforaparticularmedicineorgroupofmedicinesina
therapyareaintheassignedgeography.
2.Maintainadetailedunderstandingofthetherapyareaandadeepappreciationof
thescienceandevidenceforGSKmedicinesandothernon-GSKtreatmentoptions
inthetherapyarea.
3.Actastheinterfacebetweentheprofessionalhealthcarecommunityandthe
internalGSKmedicalteamanditsaffiliatesprovidingvalue-addedinsightsand
feedbackfromthecommunitydesignedtoimprovemedical,commercialanddrug
developmentplanningandserviceprovision.
4.Bepreparedtorespondtoanyenquiriesfromlocalhealthauthorities/tenderswith
regardtoGSKvaccinesafety/efficacy/effectivenesstoensurecoveredvacineesare
benefited,andworkcloselywithtenderandGAteamsforthecommunicationwith
HA/tenders/policymakers.
5.FullyunderstandandalwaysmeettherequirementsintheGSKStandardsfor
ScientificEngagement(POL-GSK-002andSTD-GSK-002),ExternalInteractionsby
MedicalandR&DStaff(STD-GSKF-415)and,whererelevanttopromotional
activities,theGSKCodeofPracticeforPromotionandCustomerInteractions(STD-
GSK-401).
6.Fullyunderstandandcomplywithlocalcodesofpractice,guidelinesandlawsto
ensurethestrictestrequirementsaremetparticularlywithrespecttodeliveryof
promotionalversesnon-promotionalinformation.
7.Respondcompliantlytounsolicitedinformationrequestsfromhealthcare
professionalsandassociatedindividualsregardinglicensedorun-licensedGSK
medicinesandindications;ensureallmedicalinformationresponsesarefactual,
fairandbalanced,scientificallyrigorousandstrictlycomplywithlocalregulations.
8.Disseminateimportantsafetyinformationtothehealthcareprofessionasdirected
bytheMedicalAffairsorResearchandDevelopmentteamsortheDearHealthcare
ProviderLetter(DHPL)process.
9.Assistthemedicalteamintheidentificationofexternalexpertswithinthetherapy
areaandgeography.
10.SupportGSKstudyteamswiththeprovisionofscientificeducationandenquiry
managementfrominvestigatorsandstaffengagedinGSK-supportedclinical
trialse.g.Investigator-SponsoredStudies(ISS).
11.ProvidescientificeducationtrainingforbusinesspartnerssuchastheMedical
Representatives.
待遇面議外商公司員工200人距捷運台北車站270公尺
不想看到這個公司
不想看到這個產業
儲存
應徵0~5人應徵
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