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

篇2:高級醫學顧問崗位職責

高級醫學顧問主要職責:

1.負責公司新藥腫瘤/CNS領域項目或相應平臺臨床需求調研、立項評估;

2.負責或協助公司新藥腫瘤/CNS領域項目臨床試驗方案設計、試驗報告及相關資料的撰寫或審核;

3.負責腫瘤/CNS領域臨床試驗項目醫學監查、不良事件和類似事件分析、病例報告評估,為不良事件處理提供醫學支持;

4.協助組織和召開腫瘤領域項目臨床咨詢會、研究者會議或醫學顧問委員會會議;

5.全面掌握腫瘤領域疾病和研發治療知識、臨床信息和數據,為醫學部內部人員提供相關專業知識培訓;

6.完成其它領導分配的任務。

任職要求:

1.相關專業,博士學歷,本科學歷需為5年制臨床醫學

2.有醫院臨床工作經驗者

3.熟練的中英文文獻查閱、整理、分析、綜述能力、醫學邏輯思維及運用能力

4.良好的表達能力及團隊合作精神

5.熟練使用office辦公軟件

6.年齡45周歲以下主要職責:

1.負責公司新藥腫瘤/CNS領域項目或相應平臺臨床需求調研、立項評估;

2.負責或協助公司新藥腫瘤/CNS領域項目臨床試驗方案設計、試驗報告及相關資料的撰寫或審核;

3.負責腫瘤/CNS領域臨床試驗項目醫學監查、不良事件和類似事件分析、病例報告評估,為不良事件處理提供醫學支持;

4.協助組織和召開腫瘤領域項目臨床咨詢會、研究者會議或醫學顧問委員會會議;

5.全面掌握腫瘤領域疾病和研發治療知識、臨床信息和數據,為醫學部內部人員提供相關專業知識培訓;

6.完成其它領導分配的任務。

任職要求:

1.相關專業,博士學歷,本科學歷需為5年制臨床醫學

2.有醫院臨床工作經驗者

3.熟練的中英文文獻查閱、整理、分析、綜述能力、醫學邏輯思維及運用能力

4.良好的表達能力及團隊合作精神

5.熟練使用office辦公軟件

6.年齡45周歲以下

篇3:醫學營養顧問崗位職責任職要求

醫學營養顧問崗位職責

醫學顧問/編輯(營養品領域)康斯泰克北京康斯泰克廣告有限公司,康斯泰克職位描述:

1、配合項目組的醫學支持工作,編寫產品醫學推廣材料;

2、協助項目組分析客戶的學術需求、幫助醫藥產品定位及策略制定;

3、醫學專業論文翻譯、相關文章及策劃文案撰寫;

4、與專家及制藥企業等進行學術溝通;

5、醫學前沿信息跟蹤,醫學文獻檢索,追蹤醫藥行業熱點。

職位要求:

1、基礎、臨床、營養學、預防醫學或其他醫學專業碩士及以上學歷,歡迎海內外優秀應屆生的加入;

2、具有醫學部或專業醫學編輯工作經驗為佳;

3、具有醫學專業英文翻譯,和醫學編輯能力;

4、思維活躍,知識面較寬,創新能力強;

5、良好的溝通能力及團隊合作精神;

6、具備良好的自我管理能力,能承受較強的工作壓力。

醫學營養顧問崗位