(Sr.)MACNS精神抗抑郁医学顾问工作职责与职位要求

职位描述：

职责描述：

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

编辑：www.qiquhA.com.com

篇2:高级医学顾问岗位职责

高级医学顾问主要职责:

1.负责公司新药肿瘤/CNS领域项目或相应平台临床需求调研、立项评估;

2.负责或协助公司新药肿瘤/CNS领域项目临床试验方案设计、试验报告及相关资料的撰写或审核;

3.负责肿瘤/CNS领域临床试验项目医学监查、不良事件和类似事件分析、病例报告评估,为不良事件处理提供医学支持;

4.协助组织和召开肿瘤领域项目临床咨询会、研究者会议或医学顾问委员会会议;

5.全面掌握肿瘤领域疾病和研发治疗知识、临床信息和数据,为医学部内部人员提供相关专业知识培训;

6.完成其它领导分配的任务。

任职要求:

1.相关专业,博士学历,本科学历需为5年制临床医学

2.有医院临床工作经验者

3.熟练的中英文文献查阅、整理、分析、综述能力、医学逻辑思维及运用能力

4.良好的表达能力及团队合作精神

5.熟练使用office办公软件

6.年龄45周岁以下主要职责:

1.负责公司新药肿瘤/CNS领域项目或相应平台临床需求调研、立项评估;

2.负责或协助公司新药肿瘤/CNS领域项目临床试验方案设计、试验报告及相关资料的撰写或审核;

3.负责肿瘤/CNS领域临床试验项目医学监查、不良事件和类似事件分析、病例报告评估,为不良事件处理提供医学支持;

4.协助组织和召开肿瘤领域项目临床咨询会、研究者会议或医学顾问委员会会议;

5.全面掌握肿瘤领域疾病和研发治疗知识、临床信息和数据,为医学部内部人员提供相关专业知识培训;

6.完成其它领导分配的任务。

任职要求:

1.相关专业,博士学历,本科学历需为5年制临床医学

2.有医院临床工作经验者

3.熟练的中英文文献查阅、整理、分析、综述能力、医学逻辑思维及运用能力

4.良好的表达能力及团队合作精神

5.熟练使用office办公软件

6.年龄45周岁以下

篇3:医学营养顾问岗位职责任职要求

医学营养顾问岗位职责

医学顾问/编辑(营养品领域)康斯泰克北京康斯泰克广告有限公司,康斯泰克职位描述:

1、配合项目组的医学支持工作,编写产品医学推广材料;

2、协助项目组分析客户的学术需求、帮助医药产品定位及策略制定;

3、医学专业论文翻译、相关文章及策划文案撰写;

4、与专家及制药企业等进行学术沟通;

5、医学前沿信息跟踪,医学文献检索,追踪医药行业热点。

职位要求:

1、基础、临床、营养学、预防医学或其他医学专业硕士及以上学历,欢迎海内外优秀应届生的加入;

2、具有医学部或专业医学编辑工作经验为佳;

3、具有医学专业英文翻译,和医学编辑能力;

4、思维活跃,知识面较宽,创新能力强;

5、良好的沟通能力及团队合作精神;

6、具备良好的自我管理能力,能承受较强的工作压力。

医学营养顾问岗位