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临床监查员CRA 杭州泰格医药科技股份有限公司 银川 3-4.5千/月 11-21

学历要求:本科|工作经验:1年|公司性质:合资|公司规模:1000-5000人

任职要求:Job Qualifications1、临床医学相关专业本科以上学历2、1年以上CRA相关工作经历3、对GCP及临床试验流程有一定认识4、CET-6优先1、Bachelors Degree or above,majoring in clinical medicine or related2、Minimum 1 year's CRA experience3、Good understanding and knowledge of GCP and clinical operation procedures.4、CET-6 is preferred.

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临床协调员/CRC(非全职) 北京翰兰德医药科技发展有限公司 银川 300元/天 11-21

学历要求:本科|工作经验:1年|公司性质:民营公司|公司规模:50-150人

职位描述:协助研究者完成临床试验项目的资料收集、整理和归档管理;协助研究者跟踪受试者定期随访;协调国内其他参与研究中心的工作协助研究者完成临床试验的其他相关工作。任职要求:大专或本科学历,药学,护理或临床医学专业毕业,了解药物或医疗器械临床研究的工作流程,愿意从事临床科研工作;受过GCP培训,并且有CRC、CRA工作经历1年以上。具有良好的沟通能力,良好的服务意识和团队协作精神,有责任心,积极进取,谨慎细致,条理性强;能熟练应用office等办公软件;整体形象气质良好。在所在地有固定住所。

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临床协调员 西斯比亚(北京)医药技术研究有限责任公司 银川 3.5-5千/月 11-21

学历要求:本科|工作经验:1年|公司性质:外资(欧美)|公司规模:150-500人

?* Knowledge of the protocols and through knowledge of the examinations and procedures in connection with the Study Nurse position as discussed in the protocols and in accordance with the study specific defined responsibility log.?* Thorough knowledge of CCBR procedures and quality control regulations (relevant for the Study Nurse position), which forms the basis of performing clinical studies.?* Knowledge of international/national regulations and instructions for performing clinical studies.?* Perform in a professional, kind and efficient manner, when taking care of study participants.?* Thorough knowledge to the content of the Study File and responsible for the document filling.?* Have a good grasp of the Patient File.?* Responsible for the content of the Patient File, general pages as well as study specific pages.?* Responsible for coordination concerning eligibility in the study enrolment phase.?* Update study staff members on current study procedures and other relevant information.?* Make appointments with Sponsors representative for monitoring.?* Always be updated on the current study status.?* Thorough knowledge of the time schedule.?* Handling of drug supplies.?* Handling of test results.?* Last check of Patient Files and CRF’s.?* To participate in and add information to planned clinic meetings.?* To participate in education and training planned by CCBR.?* To participate in arrangements planned by CCBR, with the purpose of nurturing the solidarity between individual demarcation groups and collaborating groups.?* To participate in subject recruitment program/community out reach.?* Participate in meetings arranged by Study Management Manager/GM; such as investigator meetings, initiation meetings etc.

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临床研究协调员(CRC) 上海百试达医药科技有限公司 银川 3-6千/月 11-15

学历要求:本科|工作经验:1年|公司性质:民营公司|公司规模:50-150人

主要职责: ? 负责受试者数据库和信息管理 ? 日常管理预约受试者的随访 ? 研究者文件夹的建立和维护? 研究文件和药品或物品的接收,发放、保存、清点和归还? 研究数据的输入和核对? 协调CRA 与研究者的沟通工作要求: 1.诚信,敬业,勤奋,踏实; 2.临床医学或药学相关专业毕业,在研究中心(医院)工作 3. 熟悉site 人际关系和工作流程; 4.较强的独立工作能力及团队合作精神 医院医生和护士***亦可!Responsibilities: -Management of subject database and information -Daily management of subjects with appointment -Creation and maintenance of investigator's folder -Receival, distribution, preservation, counting and return of research documents or drugs/substance -Input and verification of research data -Coordinate communications between CRA and Investigator Requirements: -To be faithful, dutiful, diligent and steady - Graduate of clinical medicine, pharmacy or related disciplines with prior experience in research centers (hospitals) - Be familiar with the interpersonal relationship and workflow of site -Be able to work both independently and as a team member

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