scra

该职位来源于猎聘 工作职责： 1、进行研究中心筛选访视。根据项目需求可独立对计划筛选的研究中心进行访视调研，通过对研究中心资质、设施设备、研究人员和流程等情况进行调查，撰写调查报告，及时反馈项目组供研究中心评估选择。...

该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

该职位来源于猎聘 职责描述： 1.负责临床试验各潜在中心的研究前访视； 2.协助并配合项目经理组织和召开研究者会议； 3.协助研究者进行研究中心的机构立项、伦理审查资料的准备、递交、结果跟进及批件审核归档；...

该职位来源于猎聘 1、具备肿瘤项目I-III期经验优先。 2、工作区域聚焦本地+省内短途出差，无长期异地外派、无全国频繁跑动； 3、项目管线丰富、全肿瘤项目、周期长期稳定，杜绝短期临时填坑项目，团队氛围扁平化，管理人性化；...

该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

该职位来源于猎聘 1.负责公司产品临床试验的规划、启动、执行、监查协调、数据管理与统计沟通、结题与归档； 2.管理 CRO/SMO/ 中心医院 / 伦理 / 第三方实验室 / 统计单位等外部资源，进行供应商选择、合同与绩效跟踪；...

该职位来源于猎聘 1、具备肿瘤项目I-III期经验优先。 2、工作区域聚焦本地+省内短途出差，无长期异地外派、无全国频繁跑动； 3、项目管线丰富、全肿瘤项目、周期长期稳定，杜绝短期临时填坑项目，团队氛围扁平化，管理人性化；...

该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

该职位来源于猎聘 1、具备肿瘤项目I-III期经验优先。 2、工作区域聚焦本地+省内短途出差，无长期异地外派、无全国频繁跑动； 3、项目管线丰富、全肿瘤项目、周期长期稳定，杜绝短期临时填坑项目，团队氛围扁平化，管理人性化；...

该职位来源于猎聘 Primary Responsibilities: • Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work, SOPs (and / or the Sponsor’s SOPs as appropriate) and the ICH GCP and associated regulations. May perform co-monitoring visits and other types of site visits as needed. •...

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned....

该职位来源于猎聘 岗位职责： 1.根据试验方案规定的工作范围、SOP和GCP的要求进行研究中心筛选、启动、监查和关闭访视； 2.可同时负责多个方案、研究中心和治疗领域内的研究中心监查工作；...

• 招聘类别： • 社会招聘 • 工作性质： • 全职 • 招聘人数： • 3 • 发布时间： • 2025-10-11 工作地点： 天津市,北京市 工作职责： 摘要：  高级临床监查员I/II（Sr. CRA...

SCRA ISyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.  Our Clinical Development model brings the customer and the patient to the center of everything that we do....

工作职责1.协助项目经理对公司委外研究的临床项目，包括对供应商前期考察、项目实施管理、质量管理等环节进行全面管理; 2.参与临床试验设计，协助临床经理完成CRF，ICF，招募材料等临床相关文件的审阅;3.协助维护临床研究的相关文件,协助完成研究药物的安全性数据�...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development and technology solutions across more than 20 therapeutic areas. With over 18,000 staff conducting...

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned....