第1篇 設(shè)備臨床崗位職責(zé)設(shè)備臨床職責(zé)任職要求
設(shè)備臨床崗位職責(zé)
top外資醫(yī)療器械設(shè)備臨床研究經(jīng)理crm/clinical research manager span of control (immediate subordinates’ category， number and interfaces) 負責(zé)范圍(直接下屬類別、人數(shù)及主要互動界面):
internal: global medical science affairs， regulatory affair， sales & marketing， it， finance and legal
e_ternal: hospitals， clinical research organization (cro) ， data management， statisticians， crc and other vendors
job summary (overview of job purpose) 職位概述以及職責(zé)范圍:
function as a project leader to manage and coordinate all avitum’s clinical research projects and related medical affairs.
major duties performed (main functions) 主要職責(zé):
- perform study start-up activities， including study plan build-up， study protocol and crf design， investigator meeting， ec and most approval， site selection， site initiation， e-trial development， co-monitoring， study closure and other related activities ensuring compliance with cfda regulation， gcp/ich guidelines and company sops.
- allocate the budget by project and conduct the daily management and update the usage status.
- document and updated the progress of assigned clinical studies through regular status report.
- provide direction and oversight of outsourced activities to ensure clinical research organization (cro) and vendors delivery against contracted scope of work.
-collaborate with cross functional department such as global medical science affairs， regulatory affair， sales & marketing， it， finance and legal to support project milestone achievement. provide clinical trial dossier for registration use.
- coordinate medical affairs tasks such as post marketing clinical projects， clinical evaluation report， publication.
- assist the sr. clinical research manager in building the msa network and additional responsibilities as required.
critical performance measurement 關(guān)鍵業(yè)績標(biāo)準:
- 4 ongoing clinical trials milestone achievements， accelerate the whole study duration into 1 year， optimize cro and vendor management for higher project quality.
- cross functional collaboration satisfaction.
- project management & communication skill.
education & language skills required
教育背景及語言技能要求:
bachelor/master in medical， pharmaceutical， biomedical
fluent in english
office (project management)
e_perience & special skills required
經(jīng)驗及其他特殊技能要求:
total working e_perience 8+y (5+ y sr. cra e_perience， 3+y project management)
clinical trial e_perience in medical device/pharmaceutical
cro e_perience is preferred
gcp certification， project management certificate is preferred span of control (immediate subordinates’ category， number and interfaces) 負責(zé)范圍(直接下屬類別、人數(shù)及主要互動界面):
internal: global medical science affairs， regulatory affair， sales & marketing， it， finance and legal
e_ternal: hospitals， clinical research organization (cro) ， data management， statisticians， crc and other vendors
job summary (overview of job purpose) 職位概述以及職責(zé)范圍:
function as a project leader to manage and coordinate all avitum’s clinical research projects and related medical affairs.
major duties performed (main functions) 主要職責(zé):
- perform study start-up activities， including study plan build-up， study protocol and crf design， investigator meeting， ec and most approval， site selection， site initiation， e-trial development， co-monitoring， study closure and other related activities ensuring compliance with cfda regulation， gcp/ich guidelines and company sops.
- allocate the budget by project and conduct the daily management and update the usage status.
- document and updated the progress of assigned clinical studies through regular status report.
- provide direction and oversight of outsourced activities to ensure clinical research organization (cro) and vendors delivery against contracted scope of work.
-collaborate with cross functional department such as global medical science affairs， regulatory affair， sales & marketing， it， finance and legal to support project milestone achievement. provide clinical trial dossier for registration use.
- coordinate medical affairs tasks such as post marketing clinical projects， clinical evaluation report， publication.
- assist the sr. clinical research manager in building the msa network and additional responsibilities as required.
critical performance measurement 關(guān)鍵業(yè)績標(biāo)準:
- 4 ongoing clinical trials milestone achievements， accelerate the whole study duration into 1 year， optimize cro and vendor management for higher project quality.
- cross functional collaboration satisfaction.
- project management & communication skill.
education & language skills required
教育背景及語言技能要求:
bachelor/master in medical， pharmaceutical， biomedical
fluent in english
office (project management)
e_perience & special skills required
經(jīng)驗及其他特殊技能要求:
total working e_perience 8+y (5+ y sr. cra e_perience， 3+y project management)
clinical trial e_perience in medical device/pharmaceutical
cro e_perience is preferred
gcp certification， project management certificate is preferred
第2篇 醫(yī)療器械臨床崗位職責(zé)任職要求
醫(yī)療器械臨床崗位職責(zé)
職責(zé)描述:
1、生物、醫(yī)藥、醫(yī)療器械、臨床等相關(guān)行業(yè)人員，擁有博士及以上學(xué)歷;
2、具備一定研究分析能力;
3、具有較強的溝通協(xié)調(diào)能力與執(zhí)行力;
4、對新三板及直接股權(quán)投資業(yè)務(wù)的運作和國家相關(guān)法律法規(guī)和政策有所了解;
5、能夠承受一定的工作壓力和工作強度，能適應(yīng)經(jīng)常出差;
6、具有生物、醫(yī)藥、醫(yī)療器械、臨床、金融、創(chuàng)投等相關(guān)背景。
職位描述:
1、負責(zé)項目的開發(fā)、調(diào)查、分析、制訂投資方案并進行相關(guān)商務(wù)談判;
2、負責(zé)投資項目的具體實施;
3、對已投資項目進行跟蹤管理;
4、制定項目退出方式，并負責(zé)退出的具體操作;
5、參與相關(guān)的投后管理工作。
6、完成領(lǐng)導(dǎo)交辦的其他工作。
醫(yī)療器械臨床崗位
第3篇 共振臨床崗位職責(zé)任職要求
共振臨床崗位職責(zé)
工作內(nèi)容:
1、培訓(xùn)相關(guān)科室醫(yī)生磁共振在臨床診斷上的應(yīng)用;
2、培訓(xùn)磁共振室技師磁共振各序列在臨床診斷上的選擇和應(yīng)用。
3、推廣公司品牌及產(chǎn)品，提升公司產(chǎn)品的行業(yè)影響力。
職位要求:
1、臨床醫(yī)學(xué)專業(yè)本科以上學(xué)歷;
2、醫(yī)院mri室工作經(jīng)驗2年以上;
3、有mri產(chǎn)品臨床工程師經(jīng)驗優(yōu)先;
4、能適應(yīng)長期出差。
工作內(nèi)容:
1、培訓(xùn)相關(guān)科室醫(yī)生磁共振在臨床診斷上的應(yīng)用;
2、培訓(xùn)磁共振室技師磁共振各序列在臨床診斷上的選擇和應(yīng)用。
3、推廣公司品牌及產(chǎn)品，提升公司產(chǎn)品的行業(yè)影響力。
