临床研究协调员
辽宁欧立丁医药科技有限公司
- 公司规模:50-150人
- 公司性质:民营公司
- 公司行业:制药/生物工程
职位信息
- 发布日期:2021-06-03
- 工作地点:成都
- 招聘人数:10人
- 工作经验:1年经验
- 学历要求:本科
- 语言要求:英语良好
- 职位月薪:6-8千/月
- 职位类别:临床协调员
职位描述
岗位职责:
1、依据国家相关法规、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、临床试验机构备案等工作;
3、协助及时完成SAE相关安全报告;
4、协助研究者填写病历报告表,协助研究者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,包括受试者招募、筛选潜在的受试者、 安排受试者访视、安排实验室检査、获取检査结果等;
6、协助研究者完成相关物资及药物的管理,包括接收、保存、分发、回收和归还,并完成相关记录;
7、协助CRA的中心监査工作,提前准备各种文档供CRA监査,及时全面的向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。
岗位要求:
1、临床医学或护理等相关专业、大专以上学历;
2、一年以上临床或CRC经验,有临床试验经验者优先考虑;
3、英语四级以上,良好的英文听说读写能力;
4、较强的独立工作能力及团队合作精神;
5、具备一定的抗压能力,并会自我心理调节;
6、工作积极主动,良好的沟通及应变能力。具备良好的自我学习能力。
Job Description:
1.In accordance with relevant national regulations, protocol, SOP requirements of hospital and company, and under the authorization of the investigators, assist the investigators to complete various tasks;
2.Assist investigators in completing IRB submission and clinical trial institution filing;
3.Assist in the timely completion of SAE related safety reports;
4.Assist investigators in filling out the medical record report form, and assist investigators in completing the collection, sorting and filing of documents of site at each stage of the trial;
5.Assist investigators in completing subject screening, enrollment, follow-up, etc., including subject recruitment, screening potential subjects, arranging subject visits, arranging laboratory inspections, obtaining inspection results, etc;
6.Assist researchers in the management of related supplies and IPs, including receiving, storing, dispensing, recycling and returning, and completing relevant records;
7.Assist CRA's in site monitoring, prepare various documents in advance for CRA's monitoring, and report the progress of the site to CRA in a timely and comprehensive manner;
8.Assist CRA and investigators to complete data Q&A in a timely manner;
9.Assist investigators in clinical trial management and related daily work.
Qualifications:
1.Junior college or above in medical science, nursing or related subjects;
2.Minimum 1 year of experience as a CRC or working in clinical circumstances;clinical trial experience will be plus;
3.CET 4 or above in English,and good command of English listening, speaking, reading and writing;
4.Ability to work independently,with a team spirit;
5.Ability to working under pressure and self-regulation;
6.Positive work attitude, good communication skill and adaptability to change, and strong self-learning ability.
公司介绍
联系方式
- 公司地址:地址:span三甲医院