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CRAICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.As a CRA II at ICON, you...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5...

该职位来源于猎聘 岗位职责： 1、 驻点各研究中心现场进行项目监查，确保方案正确执行，数据完整、可靠 2、 项目进度现场跟踪、推进、协调解决临床研究相关问题； 3、 风险管理：初级收集与反馈项目进行中的风险信息 4、 熟练讲解产品， 进行操作流程培训 5、...

该职位来源于猎聘 FSP Global Pharma Job responsibilities • Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate...

该职位来源于猎聘 Bachelor’s Degree in Life Sciences or an equivalent combination of education, training & experience. Certified Healthcare Professional (e.g. Registered Nurse, Licensed Practical Nurse, MD, etc) strongly preferred...

该职位来源于猎聘 Responsibilities: 1、Contribute comments/input in the development of Protocol, Informed Consent Form (ICF), Case Report Forms (CRF) and other project related documents. 2、Evaluation potential sites with the assistance from the senior CRA, PM or line manager and provide PM with recommendations for selection of qualified sites....

该职位来源于猎聘 职责描述： 1. 负责临床单位的调研、伦理递交、协议沟通及科室启动； 2. 负责临床试验项目的监查，确保负责的项目执行中符合方案、GCP、SOP和法律法规要求，确保试验数据的真实、准确、完整； • 与研究中心机构、研究者等建立良好合作关系； 4....

该职位来源于猎聘 Bachelor’s Degree in Life Sciences or an equivalent combination of education, training & experience. Certified Healthcare Professional (e.g. Registered Nurse, Licensed Practical Nurse, MD, etc) strongly preferred...

该职位来源于猎聘 职责描述： 1. 负责临床单位的调研、伦理递交、协议沟通及科室启动； 2. 负责临床试验项目的监查，确保负责的项目执行中符合方案、GCP、SOP和法律法规要求，确保试验数据的真实、准确、完整； - 与研究中心机构、研究者等建立良好合作关系；...

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；...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources...

该职位来源于猎聘 此岗位为外派上市Biotech，要求1.5年及以上CRA经验，优先实体瘤或血液肿瘤背景 主要负责血液肿瘤项目 福利、培训叠加享受CRO+申办方双重福利， 1）LM Nice 2）日常弹性工作制，不打卡 3）六险一金、年终奖、带薪假期、晋升完善

**Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...

该职位来源于猎聘 岗位职责： 1、根据项目文档管理计划、SOP、ICH-GCP/中国GCP进行项目文档管理及QC工作，并将无误的文件进行扫描保存在Sharepoint/e-TMF，确保文件的完整性和回收的及时性； 2、负责项目核心文档的基础日常管理和维护工作；...

该职位来源于猎聘 岗位职责： 1、根据项目文档管理计划、SOP、ICH-GCP/中国GCP进行项目文档管理及QC工作，并将无误的文件进行扫描保存在Sharepoint/e-TMF，确保文件的完整性和回收的及时性； 2、负责项目核心文档的基础日常管理和维护工作；...

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionMonitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data...

Summary 监控与临床研究网站和临床试验参与相关的患者数据和学习相关信息。确保调查员遵守研究协议、法规要求和良好临床实践，并为数据验证计划提供投入。提供及时和准确的监测患者数据和研究相关信息，从源文件，研究记录和现场访问（如果适用）。...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...