- 目录
第1篇 设备临床岗位职责设备临床职责任职要求
设备临床岗位职责
top外资医疗器械设备临床研究经理crm/clinical research manager span of control (immediate subordinates’ category， number and interfaces) 负责范围(直接下属类别、人数及主要互动界面):
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) 职位概述以及职责范围:
function as a project leader to manage and coordinate all avitum’s clinical research projects and related medical affairs.
major duties performed (main functions) 主要职责:
- 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 关键业绩标准:
- 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
教育背景及语言技能要求:
bachelor/master in medical， pharmaceutical， biomedical
fluent in english
office (project management)
e_perience & special skills required
经验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) 负责范围(直接下属类别、人数及主要互动界面):
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) 职位概述以及职责范围:
function as a project leader to manage and coordinate all avitum’s clinical research projects and related medical affairs.
major duties performed (main functions) 主要职责:
- 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 关键业绩标准:
- 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
教育背景及语言技能要求:
bachelor/master in medical， pharmaceutical， biomedical
fluent in english
office (project management)
e_perience & special skills required
经验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 医疗器械临床岗位职责任职要求
医疗器械临床岗位职责
职责描述:
1、生物、医药、医疗器械、临床等相关行业人员，拥有博士及以上学历;
2、具备一定研究分析能力;
3、具有较强的沟通协调能力与执行力;
4、对新三板及直接股权投资业务的运作和国家相关法律法规和政策有所了解;
5、能够承受一定的工作压力和工作强度，能适应经常出差;
6、具有生物、医药、医疗器械、临床、金融、创投等相关背景。
职位描述:
1、负责项目的开发、调查、分析、制订投资方案并进行相关商务谈判;
2、负责投资项目的具体实施;
3、对已投资项目进行跟踪管理;
4、制定项目退出方式，并负责退出的具体操作;
5、参与相关的投后管理工作。
6、完成领导交办的其他工作。
医疗器械临床岗位
第3篇 共振临床岗位职责任职要求
共振临床岗位职责
工作内容:
1、培训相关科室医生磁共振在临床诊断上的应用;
2、培训磁共振室技师磁共振各序列在临床诊断上的选择和应用。
3、推广公司品牌及产品，提升公司产品的行业影响力。
职位要求:
1、临床医学专业本科以上学历;
2、医院mri室工作经验2年以上;
3、有mri产品临床工程师经验优先;
4、能适应长期出差。
工作内容:
1、培训相关科室医生磁共振在临床诊断上的应用;
2、培训磁共振室技师磁共振各序列在临床诊断上的选择和应用。
3、推广公司品牌及产品，提升公司产品的行业影响力。
