技術(shù)協(xié)調(diào)主管崗位職責(zé)

職責(zé)描述:

oProjectmanageandcoordinatethecompilation,submissionreadyqualitycontrol,requestforsign-off,andpost-approvalcompliancerequirementsassociatedwithdevelopmentofPfizerglobalclinicalstudyreports(CSRs)

oEnsuretimelydeliveryofPfizerglobalCSRsforregulatorysubmissionsorpublicdisclosurerequirementsandensurecompliancewithregulatoryguidelines,specifications,andPfizersubmissionstandardsisachieved

oParticipateinprocessimprovementactivitiestoachieveoperationalexcellenceinclinicalstudyreportproduction

Projectmanageandcoordinatecompilation,qualitycontrol,approvalandpost-approvalprocessesassociatedwithdevelopmentofPfizerglobalCSRs,including:

oCreateCSRmockupsinPfizerDocumentManagementSystemandpopulatedocumenttemplates

oProjectmanageCSRcompilation,approvalandpublishingactivities

oExecutesubmissionreadyQConCSRcomponentsandstructure

oCommunicatewithsuppliersregardingissueswithCSRcomponentsandseekresolutions

oSeekapprovalfromsignatoriesonfinalizedCSRsandupdateclinicaltrialregistrywithCSRmilestonestatus

oPrepareinvestigator’sdeclarationpackagesfordistributiontothecoordinatinginvestigator

oPreparestudydatapackagesrequiredfordistributiontostudyPIs

Generally:

oEnsureallCSRactivitiesareexecutedwithinagreedtimelinesandinaccordancewithworkingpractices.

oProactivelyestablishandfollowclearprioritiesacrossportfolioofCSRworkloadtoensurethetimelycompletionofCSRscontributingtoaregulatorysubmission.

oWhereapplicable,provideappropriateresponsestoanyauditfindings.

oActivelypursuetrainingintechnicalandpersonalskillsrelevanttotheCSRCoordinatorrole.

oContributetotheachievementofdepartmentalgoalsbyensuringthattargetsareincorporatedintoteamandpersonalgoals,andensurethatrelevantmetricsarecollectedsothatfunctionallinecanmonitorandaddressgoals,targetsandSubmissionReadyissues.

oInpursuitofmaximumefficiencythataddressesbothspeedandqualityindocumentpreparationacrossalltherapeuticareas,assurethatlessonslearnedaresharedandappliedacrossprograms,andcarryoutestablishedstrategiestoachievecontinuousprocessimprovementtowardsexcellenceindocumentmanagement.

oWhereappropriate,actasmentorstonewlyappointedCSRCoordinators

任職要求:

TechnicalSkillRequirements

oAttentiontodetailandexceptionalorganizationalskills

oProficiencyinEnglishlanguage(read,writtenandspoken)

oTrackrecordofexcellenceincoordinationskills

oExperienceinclinicalstudyoperationsorregulatoryoperationspreferred

oExperienceinprojectmanagementpreferred

oExperienceinelectronicdocumentmanagementpreferred

Experienceinmultinationalcompanypreferred

Qualifications(i.e.,preferrededucation,experience,attributes)

Masterorbachelordegreeinbiological,medical,orpharmaceuticalsciencespreferred

篇2:經(jīng)理協(xié)調(diào)主管崗位職責(zé)任職要求

經(jīng)理協(xié)調(diào)主管崗位職責(zé)

崗位職責(zé):

1、負(fù)責(zé)化妝品OEM訂單承接;

2、原物料交期和生產(chǎn)排程跟催,出貨協(xié)調(diào);

3、物料消耗核算等化妝品外加工環(huán)節(jié)的跟進(jìn)落實;

4、熟悉OEM業(yè)務(wù)流程、具備項目管理經(jīng)驗,熟悉日化產(chǎn)品生產(chǎn)流程、報價議價及相關(guān)法規(guī)。

任職資格:

1、全日制本科以上學(xué)歷;

2、化工及工商管理類相關(guān)專業(yè);

3、2年以上化妝品OEM業(yè)務(wù)管理工作經(jīng)驗;

4、良好的口頭、書面溝通能力,電腦文檔編輯及數(shù)據(jù)分析處理能力。崗位職責(zé):

1、負(fù)責(zé)化妝品OEM訂單承接;

2、原物料交期和生產(chǎn)排程跟催,出貨協(xié)調(diào);

3、物料消耗核算等化妝品外加工環(huán)節(jié)的跟進(jìn)落實;

4、熟悉OEM業(yè)務(wù)流程、具備項目管理經(jīng)驗,熟悉日化產(chǎn)品生產(chǎn)流程、報價議價及相關(guān)法規(guī)。

任職資格:

1、全日制本科以上學(xué)歷;

2、化工及工商管理類相關(guān)專業(yè);

3、2年以上化妝品OEM業(yè)務(wù)管理工作經(jīng)驗;

4、良好的口頭、書面溝通能力,電腦文檔編輯及數(shù)據(jù)分析處理能力。