- 目录
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第1篇 临床医学专员岗位职责
临床医学专员/经理 职位描述:
1.根据临床试验要求,负责设计及报告撰写阶段的文献检索查询相关医学、药信息和参考文献,提供相关信息;
2.参与临床试验方案讨论,撰写或修改、病例报告表知情同意书等;
3.负责临床研究总结报告的撰写;
4.协助商务部门项目投标的医学支持、临床试验研究方案摘要等相关文件撰写。
任职要求 :
1.临床医学 、药相关专业硕士学 历,有医学撰写经验者优先;
2.英语读写流利,能够熟练阅和翻译医学、药方面专业文献;
3.能够熟练使用医学、药专业文献检索工具;
4. 善于沟通,具有良好的团队合作精神。 职位描述:
1.根据临床试验要求,负责设计及报告撰写阶段的文献检索查询相关医学、药信息和参考文献,提供相关信息;
2.参与临床试验方案讨论,撰写或修改、病例报告表知情同意书等;
3.负责临床研究总结报告的撰写;
4.协助商务部门项目投标的医学支持、临床试验研究方案摘要等相关文件撰写。
任职要求 :
1.临床医学 、药相关专业硕士学 历,有医学撰写经验者优先;
2.英语读写流利,能够熟练阅和翻译医学、药方面专业文献;
3.能够熟练使用医学、药专业文献检索工具;
4. 善于沟通,具有良好的团队合作精神。
第2篇 临床信息专员岗位职责任职要求
临床信息专员岗位职责
临床信息专员 1、客诉信息的接受、跟踪、了解、分析。
2、客诉问题和各部门及时沟通，在临床角度给出产生客诉的可能
3、审查客诉诊断报告并给出到相关人员
4、必要时和客户见面了解信息，给出客诉诊断。
5、在产品立项、研究等情况时，给出相关临床意见
6、跟踪新产品的动物实验、临床试验，试用、使用情况，并给出意见。
7、参与质量改善，给出临床方面意见
8、完成宣传产品等其他相关任务。
要求10年以上外科医生经验，岗位相当于技术顾问，从医生的角度给产品指导及根据反馈给出合理建议 1、客诉信息的接受、跟踪、了解、分析。
2、客诉问题和各部门及时沟通，在临床角度给出产生客诉的可能
3、审查客诉诊断报告并给出到相关人员
4、必要时和客户见面了解信息，给出客诉诊断。
5、在产品立项、研究等情况时，给出相关临床意见
6、跟踪新产品的动物实验、临床试验，试用、使用情况，并给出意见。
7、参与质量改善，给出临床方面意见
8、完成宣传产品等其他相关任务。
要求10年以上外科医生经验，岗位相当于技术顾问，从医生的角度给产品指导及根据反馈给出合理建议
临床信息专员岗位
第3篇 临床维护专员岗位职责
岗位职责:负责客情关系的维护工作;负责产品的进一步讲解和临床销售;负责其余科室的宣传维护工作;岗位要求:有过相关工作经验者优先,并且待遇优厚!学医或从事护理专业方面的优先!
第4篇 cra临床研究专员岗位职责
临床研究专员/cra- 上海 达孜县君合科技有限公司 达孜县君合科技有限公司,君合医药,君合科技,君合 职位描述:
按照要求协助或负责i~iv 期临床研究中的各项工作,对新药研发流程及临床研究相关法律法规有一定了解。在临床研究经理或项目经理指导下,能够负责研究中心的日常管理工作,独立进行监查工作。
任职资格:
1. 临床医学、药学或相关专业学历,对药品管理有关法规、临床研究和临床研究监查流程有一定了解。
2. 一年以上临床研究监查工作经验,进行过独立的临床研究监查。
3. 具备一定的沟通表达能力、判断能力、应变能力及问题解决能力。
4. 良好的写作能力及组织能力,能够根据工作分配的强度及优先度进行自我调整。
5. 积极主动的工作态度,能适应长期出差。
6. 熟练的使用windows操作系统与office系列办公软件包括word、e_cel、powerpoint。
7. 具备一定的英语阅读及写作能力。
第5篇 临床专员岗位职责
临床专员 博毅雅(上海)医疗科技有限责任公司 博毅雅(上海)医疗科技有限责任公司,博毅雅 工作职责:
1、 为客户或部门内部提供产品知识培训及临床应用培训;
2、 协助产品推广,向用户现场演示和介绍产品、临床应用的方法;
3、 收集临床资料和用户需求反馈,研究总结临床应用优势和新的产品应用领域。
4、 帮助销售人员和代理商更好地理解产品的临床应用。
5、 与国内、国外的业内专家建立联系,为公司产品开发提供临床理论支持。
任职资格:
1、具有医学背景及临床实践背景;
2、善于沟通,有应急事件处理能力,高度的责任感及对外协调能力。
3、较强的学习能力和上进心心。
第6篇 临床协调专员岗位职责
cra(临床试验协调专员) 欣凯医药化工中间体 欣凯医药化工中间体(上海)有限公司,欣凯医药,欣凯医药化工中间体,欣凯 岗位职责:
1.根据gcp及公司sop执行临床监查工作;
2.确保试验严格按照方案、gcp及相关法律法规执行;
3.协助研究中心解决试验过程中可能出现的问题;
4.确保研究数据及时、准确、完整地记录在原始病历中,病例报告表与原始病历数据一致;
5.及时全面地汇报研究中心进展情况;
6.完成相应书面工作;
7.协助研究者及时完成数据疑问;
8.及时、完整地收集研究相关资料;
9.完成试验结束阶段的药品、资料整理与回收,关闭中心。
任职要求:
1. 临床医学、药学等相关专业本科及本科以上学历;有临床风湿病工作经验优先;
2. 一年以上临床监查工作经验;
3. 熟悉临床试验监查、fda、cfda法规、ich/gcp条例;
4.与人沟通、谈判、表达能力较强。
第7篇 临床销售专员岗位职责任职要求
临床销售专员岗位职责
【长沙_临床微生物】客户专员/销售代表 responsibility:
-sales targets: actively complete assigned territory core instrument/reagent business sales tasks through field clinical communication in relevant departments of hospitals
-customer management: implement field clinical communication and utilize the bd academic platform and the speaker pools to influence the customers in territory for business.
-strictly abide by country compliance law and bd policy and rules.
-visit target customers regularly according to the specified scope and do the micro-market analysis for the assigned hospitals. target customer includes clinical laboratory director， micro-biology team leader， relevant clinical department doctors and nurses， infection & control department director， equipment director， vice president and president.
- make sales/marketing strategy against competitors together with marketing and as team.
-be participant into professional education branding establishment of ds， enhance self-capabilities， especially on knowledge of microbiology， to be an e_pert in microbiology industrial. responsibility:
-sales targets: actively complete assigned territory core instrument/reagent business sales tasks through field clinical communication in relevant departments of hospitals
-customer management: implement field clinical communication and utilize the bd academic platform and the speaker pools to influence the customers in territory for business.
-strictly abide by country compliance law and bd policy and rules.
-visit target customers regularly according to the specified scope and do the micro-market analysis for the assigned hospitals. target customer includes clinical laboratory director， micro-biology team leader， relevant clinical department doctors and nurses， infection & control department director， equipment director， vice president and president.
- make sales/marketing strategy against competitors together with marketing and as team.
-be participant into professional education branding establishment of ds， enhance self-capabilities， especially on knowledge of microbiology， to be an e_pert in microbiology industrial.
临床销售专员岗位
第8篇 临床协调专员岗位职责任职要求
临床协调专员岗位职责
岗位职责:
1.根据gcp及公司sop执行临床监查工作;
2.确保试验严格按照方案、gcp及相关法律法规执行;
3.协助研究中心解决试验过程中可能出现的问题;
4.确保研究数据及时、准确、完整地记录在原始病历中，病例报告表与原始病历数据一致;
5.及时全面地汇报研究中心进展情况;
6.完成相应书面工作;
7.协助研究者及时完成数据疑问;
8.及时、完整地收集研究相关资料;
9.完成试验结束阶段的药品、资料整理与回收，关闭中心。
任职要求:
1. 临床医学、药学等相关专业本科及本科以上学历;有临床风湿病工作经验优先;
2. 一年以上临床监查工作经验;
3. 熟悉临床试验监查、fda、cfda法规、ich/gcp条例;
4.与人沟通、谈判、表达能力较强。
临床协调专员岗位
第9篇 临床学术专员岗位职责任职要求
临床学术专员岗位职责
职责描述:
1、负责所辖区域肝病检测项目的推广和销售工作;
2、根据公司销售和开发目标，完成所辖区域的销售和开发目标;
3、负责客户信息的收集和上报，完成客户业务合同的签订;
4、负责所辖区域内销售活动的策划和执行;
5、负责所辖区域内的应收账款的回款及上级安排的其他相关工作。
任职要求:
1、医学或营销类相关专业;
2、从事医疗行业销售工作1年以上，曾有过医学检测、肝病线药品销售相关经验者优先;
3、具备良好的沟通表达能力及团队合作精神;
4、勤奋敬业、工作热情主动、善于思考、执行力强。
临床学术专员岗位
第10篇 临床医学专员岗位职责要求
职位描述：
岗位职责：
1、医学病历撰写、整理，影像资料的识别和分类；
2、客户就医完成后资料的整理和上传，定期的随访跟踪，跟踪记录的汇集和总结，指导进一步检查检验；
3、高端客户健康管理资料建立和方案制定；
4、负责通过检索文献获得国外医疗前沿信息等；
5、公司领导安排的其他工作；
岗位要求：
1、临床医学或相关专业本科以上学历，硕士以上优先；
2、1年以上医院临床工作经历优先；
3、英语读写能力较好，具备专业医学文献的检索、阅读和分析能力，具有方案、文章撰写能力者优先；
4、工作主动，认真负责，有较强的学习能力
第11篇 临床事务专员岗位职责
临床事务专员 1、检索产品临床相关信息(包括但不限于:产品的临床试验情况、不良事件等);
2、负责产品说明书编写;
3、负责临床试验机构筛选;
4、负责与统计学专家和临床专家沟通草拟临床方案,及临床方案的修改;
5、负责研究者手册和/或临床试验须知、知情同意书、病例报告表等相关临床文件编写和修改;
6、负责组织研究者(方案讨论会)会议;
7、协助cra与伦理委员会和临床试验机构沟通;
8、协助cra进行临床试验启动会准备及研究者培训;
9、负责汇总整理临床试验产品使用性能反馈,并将反馈信息提交给项目经理;
10、负责统计报告核查,确保统计报告符合临床试验方案要求;
11、负责临床总结报告编写、与研究者沟通;
12、负责组织解决国家食品药品监督管理局医疗器械技术审评中心评审发补意见中临床部分工作。 可接受应届毕业生 1、检索产品临床相关信息(包括但不限于:产品的临床试验情况、不良事件等);
2、负责产品说明书编写;
3、负责临床试验机构筛选;
4、负责与统计学专家和临床专家沟通草拟临床方案,及临床方案的修改;
5、负责研究者手册和/或临床试验须知、知情同意书、病例报告表等相关临床文件编写和修改;
6、负责组织研究者(方案讨论会)会议;
7、协助cra与伦理委员会和临床试验机构沟通;
8、协助cra进行临床试验启动会准备及研究者培训;
9、负责汇总整理临床试验产品使用性能反馈,并将反馈信息提交给项目经理;
10、负责统计报告核查,确保统计报告符合临床试验方案要求;
11、负责临床总结报告编写、与研究者沟通;
12、负责组织解决国家食品药品监督管理局医疗器械技术审评中心评审发补意见中临床部分工作。
第12篇 临床研究项目专员岗位职责
临床研究经理-项目经理-主管-专员 main tasks & responsibilities
1. contribute country specific aspects in the development of protocol, protocol revisions, amendments and crf design;
2. responsible for the management of designated sites in clinical trial including:
site assessment; preparation of the monitoring plan and e_ecution in compliance with visit frequency and all assigned tasks throughout the study; planning and e_ecution of study logistics plan, including eventual delegation of activities to support group; safety and proper conduct throughout the trial.
3. site specific data management;
4. prepare documentation for irb/ec submission/approval, together with study management per country specific requirements;
5. prepare and review clinical study agreements and budgets with study manager and contracts group;
6. ensure procedures are in place for appropriate enrollment of patients into the clinical trial;
7. organize investigator’s start-up meeting and study site initiation meetings, including training of the e_ternal study personnel in the use of the instruments and reagents and software packages for the on-line data capture and for the computer based e.g. with wincaev and training in the use of electronica crfs with remote data entry;8. responsible for instrument installation, check and validation (internal and e_ternal) for system study. if applicable, prepare workflow sheet for system studies, together with study management;
9. responsible for logistics of required evaluation/clinical trial material. informs and monitors sites for correct storage conditions;
10. preparation of all study binders;
11. perform investigator training (compliance & technical part).
12. verify the investigator follows the approved protocol and all gcp procedures;
13. verify all research staff and facilities have adequate qualifications and resources remain adequate throughout the duration of the study;
14. key contact for communications between the sponsor and the investigator; the point of first contact when investigators/site personnel enquire about patient inclusion/e_clusion criteria for ongoing trials;
15. ensure that observations during studies are correctly tracked and forwarded to the responsible departments in ____;
16. verify that source data/documents and other trial records are accurate, complete, and maintained. regarding the result calculations: ensure the usability of validated computer programs/software and result calculation in compliance to applicable sops;17. communicate deviations from the protocol, sops, gcp, and the applicable regulatory requirements to the investigator;
18. interprets and evaluates results with respect to the study goals and, if necessary, discuss with the site, the study manager, eg. interruption of the study or initiation of additional measurements at the e_ternal site;
19. perform troubleshooting for une_pected results according to study manager or protocol’s requirements;
20. ensure completion and availability of study documentation, together with study management;21. adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol;22. conduct study close-out visits according to monitoring plan;
23. ensure ecrf and wincaev are ready for database lock;
24. archive study records / database according to guidelines;
25. responsible for post study sample/reagents/investigational use products/instruments disposition completed during the close-out visit;26. participation in project teams, global conference calls and/or meetings to review progress of ongoing clinical trials and to assess development of new projects regarding customer usability, practicability and sop development, to continuously improve quality and efficiency of the evaluation team and processes;
27. contribute to the content of the study report and contribute to publications for journals and congresses.
possible additional tasks for senior position holders;
28. responsible for investigator selection (accountability lies with study manager)
29. provide mentoring, including training on the job, to the new cras to ensure that their role and contribution is optimized.
basic requirements of the job
1. bio-medical related scientific degree; can vary from a bachelor, master and nursing qualifications;
2. knowledge of applicable standards an regulations for clinical trials and lab conduct (international conference on harmonization / who good clinical practice standards (ich-gcp), ivd directives, fda regulations)
3. practical e_perience in study monitoring according to global standards (ich)
4. 2-5 years of clinical laboratory e_perience;
5. demonstrated e_perience in computer skills to include microsoft word, e_cel, and basic templates;
6. basic statistical knowledge;
7. professional use of the english language; both written and oral;
8. open and clear communicator;
9. ability to make sound decisions and analyze and solve problems;
10. conscientious and precise delivery of work even when under pressure jd 为参考。经理-专员各级别都有。
背景优先级:1 ivd 2 cro 3 器械 4 药 main tasks & responsibilities
1. contribute country specific aspects in the development of protocol, protocol revisions, amendments and crf design;
2. responsible for the management of designated sites in clinical trial including:
site assessment; preparation of the monitoring plan and e_ecution in compliance with visit frequency and all assigned tasks throughout the study; planning and e_ecution of study logistics plan, including eventual delegation of activities to support group; safety and proper conduct throughout the trial.
3. site specific data management;
4. prepare documentation for irb/ec submission/approval, together with study management per country specific requirements;
5. prepare and review clinical study agreements and budgets with study manager and contracts group;
6. ensure procedures are in place for appropriate enrollment of patients into the clinical trial;
7. organize investigator’s start-up meeting and study site initiation meetings, including training of the e_ternal study personnel in the use of the instruments and reagents and software packages for the on-line data capture and for the computer based e.g. with wincaev and training in the use of electronica crfs with remote data entry;8. responsible for instrument installation, check and validation (internal and e_ternal) for system study. if applicable, prepare workflow sheet for system studies, together with study management;
9. responsible for logistics of required evaluation/clinical trial material. informs and monitors sites for correct storage conditions;
10. preparation of all study binders;
11. perform investigator training (compliance & technical part).
12. verify the investigator follows the approved protocol and all gcp procedures;
13. verify all research staff and facilities have adequate qualifications and resources remain adequate throughout the duration of the study;
14. key contact for communications between the sponsor and the investigator; the point of first contact when investigators/site personnel enquire about patient inclusion/e_clusion criteria for ongoing trials;
15. ensure that observations during studies are correctly tracked and forwarded to the responsible departments in ____;
16. verify that source data/documents and other trial records are accurate, complete, and maintained. regarding the result calculations: ensure the usability of validated computer programs/software and result calculation in compliance to applicable sops;17. communicate deviations from the protocol, sops, gcp, and the applicable regulatory requirements to the investigator;
18. interprets and evaluates results with respect to the study goals and, if necessary, discuss with the site, the study manager, eg. interruption of the study or initiation of additional measurements at the e_ternal site;
19. perform troubleshooting for une_pected results according to study manager or protocol’s requirements;
20. ensure completion and availability of study documentation, together with study management;21. adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol;22. conduct study close-out visits according to monitoring plan;
23. ensure ecrf and wincaev are ready for database lock;
24. archive study records / database according to guidelines;
25. responsible for post study sample/reagents/investigational use products/instruments disposition completed during the close-out visit;26. participation in project teams, global conference calls and/or meetings to review progress of ongoing clinical trials and to assess development of new projects regarding customer usability, practicability and sop development, to continuously improve quality and efficiency of the evaluation team and processes;
27. contribute to the content of the study report and contribute to publications for journals and congresses.
possible additional tasks for senior position holders;
28. responsible for investigator selection (accountability lies with study manager)
29. provide mentoring, including training on the job, to the new cras to ensure that their role and contribution is optimized.
basic requirements of the job
1. bio-medical related scientific degree; can vary from a bachelor, master and nursing qualifications;
2. knowledge of applicable standards an regulations for clinical trials and lab conduct (international conference on harmonization / who good clinical practice standards (ich-gcp), ivd directives, fda regulations)
3. practical e_perience in study monitoring according to global standards (ich)
4. 2-5 years of clinical laboratory e_perience;
5. demonstrated e_perience in computer skills to include microsoft word, e_cel, and basic templates;
6. basic statistical knowledge;
7. professional use of the english language; both written and oral;
8. open and clear communicator;
9. ability to make sound decisions and analyze and solve problems;
10. conscientious and precise delivery of work even when under pressure
第13篇 临床项目专员岗位职责
临床项目启动专员ssu 北京斯丹姆赛尔技术有限责任公司 北京斯丹姆赛尔技术有限责任公司,斯丹姆赛尔 岗位职责
1.根据试验方案、合同规定的工作范围、sop和gcp的要求进行研究中心筛选、伦理递交、合同谈判和核心文件准备等工作。
2.可同时负责多个项目、研究中心和治疗领域内的研究中心启动工作。
3.对所负责的研究中心进行方案和研究相关的沟通,为项目筛选合适的研究中心。
4.负责研究中心临床试验协议的谈判与签署工作。
5.负责协调研究中心启动所需核心文件的收集、审阅、批准等工作。
6.负责研究中心伦理文件准备、递交、沟通等工作,并协助取得伦理批件。
7.协助研究中心启动前药品及试验物资的准备及分发工作。
8.通过追踪注册申报和批复、递交及批准文件的沟通信、电话沟通等,管理所负责研究中心的
进展。
9.负责相应研究中心启动阶段的研究财务管理。
10.协助进行项目的可行性调研。
11.与其他职能部门共同合作。
12.完成直线经理和/或项目经理(pm)分配的其他工作。
岗位要求
1.临床医学、药理学、护理学、卫生管理或其他相关专业的大专以上学历。
2.1年以上临床研究、临床监查、临床项目启动或临床协调员经验。
3.良好的临床研究知识,了解相关的法规要求。
4.通过公司培训,掌握方案要求的知识。
5.良好的计算机技能,包括熟练应用微软word、e_cel和powerpoint,以及熟练使用手提电脑。
6.良好的口头和书面沟通能力。
第14篇 临床数据专员职位描述与岗位职责任职要求
职位描述：
岗位职责:
1. 参与数据库和核查程序测试
2. 按照数据核查计划核查数据，解决数据质疑，对数据进行清理
3. 进行严重不良事件和外部数据的一致性核查
4. 准备数据审阅会议资料，参与数据审核会议
5. 协助项目数据经理进行数据库锁定
6. 数据库及相关管理文件的归档
7. 完成项目数据经理分配的其余工作
任职要求：
1. 临床医学、护理学、药学及相关专业专科以上学历（接受应届生）；
2. 良好的英语阅读能力；
3. 工作认真、负责、细心；
4. 有良好的表达沟通能力、学习能力和接受能力；
5. 了解和遵守核心的工作流程和工作指导；
第15篇 临床信息专员岗位职责
临床信息专员 风和医疗器材 江苏风和医疗器材股份有限公司,fengh medical,江苏风和,风和医疗,风和医疗器材,风和 1、客诉信息的接受、跟踪、了解、分析。
2、客诉问题和各部门及时沟通,在临床角度给出产生客诉的可能
3、审查客诉诊断报告并给出到相关人员
4、必要时和客户见面了解信息,给出客诉诊断。
5、在产品立项、研究等情况时,给出相关临床意见
6、跟踪新产品的动物实验、临床试验,试用、使用情况,并给出意见。
7、参与质量改善,给出临床方面意见
8、完成宣传产品等其他相关任务。
第16篇 临床项目专员岗位职责任职要求
临床项目专员岗位职责
岗位职责:
1、根据时间表管理临床项目执行层面的各项支持工作;
2、熟练使用科技手段支持临床试验项目在ctms和etmf中的管理;
3、成为临床试验管理系统的使用专家并承担管理员职责;
4、支持临床试验团队进行etmf的归档和整理;
5、负责与公司财务进行项目相关乃至运营相关的沟通和操作;
6、支持项目经理进行供应商管理;
7、组织各类研究者会议并统筹会务工作。
职位要求:
1、大学本科以上，医药相关专业，英文读写流利;
2、应届毕业生，有相关工作经验者优先;
3、具有计算机相关基础知识，愿意学习新的线上程序和系统的应用;
4、具有基本的药物研发知识，基本了解临床试验过程和对相关文件的要求;
5、 良好的沟通、表达和执行能力，善于团队合作，认真负责、严谨稳健。
临床项目专员岗位
