职位&公司对比
职位详情
- 枣庄
- 1年以内
- 不限
- 一期临床试验
- 二期临床试验
- 三期临床试验
- 药学专业背景
- 医学专业背景
- 护理相关背景
岗位职责: 1. 依据国家相关GCP法规、研究方案、医院及公司SOP要求, 在研究者的授权下,协助研究者完成各项工作: 2. 协助研究者完成伦理资料递交、临床试验机构立项等工作; 3. 协助研究者完成患者的管理等工作; 4. 协助研究者填写病例报告表,完成试验各个阶段研究中心的文档收集、整理、归档; 5. 协助研究者完成受试者筛选、入组、随访等工作,包括患者的知情同意、筛选潜在的受试者、安排受试者访视、安排实验室检查、获取检查结果等; 6. 协助研究者完成临床boss研究器械及其相关物资的管理,包括接收、保存、分发、回收和归还,并完成相关记录; 7. 协助CRA的中心监查工作,提前准备各种文档供CRA监查,及时全面地向CRA汇报研究中心进展情况; 8. 协助CRA、研究者及时完成数据答疑; 9. 协助研究者进行临床试验管理及相关日常工作。 10. 公司指派的其他工作。 任职要求: 1. 临床医学、药学、护理学等医疗卫生相关专业 2、大专或以上学历,职业规划清晰 3. 熟练使用Word, Excel等office办公软件; 4. 很强的工作责任心,有关注细节的工作习惯; 5. 工作积极主动,良好的沟通协调能力和承受工作压力; 6. 良好的时间管理和解决问题的能力,具有奉献精神,能够接受短期出差。 7. 较强的独立工作能力及良好的团队合作精神; 8. 有相关经验、GCP证书者优先考虑 Responsibilities: 1. According to the relevant national GCP regulations, research protocols, hospital and company SOP requirements, under the authorization of the research来自BOSS直聘er, assist the researcher to complete the work: 2. Assist the investigator to complete the ethical data submission, clinical trial project approval, etc; 3. Assist investigator to complete the management of patients; 4. Assist the 来自BOSS直聘investigatorBOSS直聘 to fill in the case report form and complete the document collection, sorting and filing of the research center at each stage of the trial; 5. Assist investigator to complete the work of subject selection, enrollment and follow-up, including inforkanzhunmed consent of patients, screening potential subjects, arranging subject visit, arranging laboratory examination, obtaining examination results, etc; 6. Assist investigator to complete the management of clinical research instruments and related materials, including receiving, saving, distributing, recycling and returning, and complete relevant records; 7. Assist CRA's central audit, prepare various documents in advance for CRA's audit, and report the progress of the research center to CRA in a timely and comprehensive manner; 8. Assist CRA and researchers to complete data answering in time; 9. Assist investigators in clinical trial management and related daily work. 10. Other work assigned by the company. Requirements: 1. Clinical medicine, pharmacy, nursing and other medical and health related majors 2. College degree or above, clear career planning 3. Proficient in using office software such as word and excel; 4. Have a strong sense of responsibility and work habit of paying attention to details; 5. Work actively, good communication and coordination ability, and work under pressure; 6. Good time management and problem solving ability;Dedicated and able to take short-term business trip. 7. Strong ability to work independently and good team spirit; 8. Relevant experience and GCP certificate are preferred
职位详情
- 枣庄
- 1-3年
- 大专
- GCP证书
- 二期临床试验
- 医学专业背景
- 三期临床试验
- 一期临床试验
- 护理相关背景
- 上市后临床试验
- 药学专业背景
岗位职责: 1. 依据国家相关GCP法规、研究方案、医院及公司SOP要求, 在研究者的授权下,协助研究者完成各项工作: 2. 协助研究者完成伦理资料递交、临床试验机构立项等工作; 3. 协助研究者完成患者的管理等工作; 4. 协助研究者填写病例报告表,完成试验各个阶段研究中心的文档收集、整理、归档; 5. 协助研究者完成受试者筛选、入组、随访等工作,包括患者的知情同意、筛选潜在的受试者、安排受试者访视、安排实验室检查、获取检查结果等; 6. 协助研究者完成临床研究器械及其相关物资的管理,包括接收、保存、分发、回收和归还,并完成相关记录; 7. 协助CRA的中心监查工作,提前准备各种文档供CRA监查,及时全面地向CRA汇报研究中心进展情况; 8. 协助CRA、研究者及时完成数据答疑; 9. 协助研究者进行临床试验管理及相关日常工作。 10. 公司指派的其他工作。 任职要求: 1. 临床医学、药学、护理学等医疗卫生相关专业 2、大专或以上学历,职业规划清晰 3. 熟练使用Word, Excel等office办公软件; 4. 很强的工作责任心,有关注细节的工作习惯; 5. 工作积极主动,良好的沟通协调能力和承受工作压力; 6. 良好的时间管理和解决问题的能力,具有奉献精神,能够接受短期出差。 7. 较强的独立工作能力及良好的团队合作精神; 8. 有相关boss经验、GCP证书者优先考虑 Responsibilities: 1. According to the relevaBOSS直聘nt national GCP regulations, research protocols, hospital and company SOP rebossquirements, under the authorization of the researcher, assist the researcher to complete the work: 2. Assist the investigator to complete the ethical data submission, clinical trial project approval, etc; 3. Assist investigator to complete the management of patients; 4. Assist the investigator to fill in the case report form and complete the document collection, sorting and filing of the research center at each stage of the trial; 5. Assist investigator to complete the work of subject selection, enrollment and follow-up, including informed consent of patients, screening potential subjects, arranging subject visit, arranging laboratory examination, obtaining examination results, etc; 6. Assist investigator to complete the management of clinical research instruments and related materials, including receiving, saving, distributing, recycling and returning, and complete relevant recoBOSS直聘rds; 7. Assist CRA's central audit, prepare various documents in advance for CRA's audit, and report the progress of the research center to CRA in a timely and comprehensive manner; 8. Assist CRA and researchers to complete data answering in time; 9. Assist investigators in clinical trial management and related daily work. 10. Other work assigned by the company. Requirements: 1. Clinical medicine, pharmacy, nursin直聘g and other medical and health related majors 2. College degree or above, clear career planning 3. Proficient in using office software such as word and excel; 4. Have a strong sense of responsibility and work habit of paying attention to details; 5. Work actively, good communication and coordination ability, and work under pressure; 6. Good time management and problem solving ability;Dedicated and able to take short-term business trip. 7. Strong ability to work independently and good team spirit; 8. Relevant experience and GCP certificate are preferred
技能解析
- 进展情况
- 团队合作精神
- 办公软件
- 解决问题的能力
- 临床研究
- 沟通协调
- 解决问题
- 临床试验
- 团队合作
- 协调能力
- 沟通协调能力
- 临床医学
- 合作精神
- 好的沟通
- 研究方案
- 良好的沟通协
数据来自CSL职业科学研究室
技能解析
- 进展情况
- 团队合作精神
- 办公软件
- 解决问题的能力
- 临床研究
- 沟通协调
- 解决问题
- 临床试验
- 团队合作
- 协调能力
- 沟通协调能力
- 临床医学
- 合作精神
- 好的沟通
- 研究方案
- 良好的沟通协
数据来自CSL职业科学研究室
工作时间
工作时间
公司福利
- 交通补助
- 节日福利
- 通讯补贴
- 员工旅游
- 带薪年假
- 绩效奖金
- 年终奖
- 定期体检
- 意外险
- 补充医疗保险
- 五险一金
公司福利
- 交通补助
- 节日福利
- 通讯补贴
- 员工旅游
- 带薪年假
- 绩效奖金
- 年终奖
- 定期体检
- 意外险
- 补充医疗保险
- 五险一金