Shanghai今日更新的90个cra职位机会
个职位
· 页 1 / 5Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Trainee Clinical Research Associate (CRA) – 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
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, clea
传思译奥（上海）商贸有限公司该职位来源于猎聘 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 生命科学专业或具有相关行业经验，本科以上学历。医疗行业注册人员（例如注册护士，执业护士等）优先考虑 Excellent oral and written c
该职位来源于猎聘 FSPxTop Global Pharma 负责Global II/III期肿瘤项目 JOB SUMMARY The Clinical Research Associate (CRA) will perform monitoring and site management activities for Phase I-IV clinical research projects to assess the progress of clinical projects at assigned investigative/physician sites (either on site
赛纽仕医药咨询(上海)有限公司该职位来源于猎聘 FSP global Biotech 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. Use
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Trainee Clinical Research Associate (CRA) – 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
传思译奥（上海）商贸有限公司该职位来源于猎聘 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 生命科学专业或具有相关行业经验，本科以上学历。医疗行业注册人员（例如注册护士，执业护士等）优先考虑 Excellent oral and written c
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, clea
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Trainee Clinical Research Associate (CRA) – 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 clinic
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Trainee Clinical Research Associate (CRA) – 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 clinic
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Trainee Clinical Research Associate (CRA) – 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 clinic
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Trainee Clinical Research Associate (CRA) – 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 clinic
该职位来源于猎聘 岗位职责： 协助项目经理管理3-5个临床试验项目，确保项目进度符合GCP要求 负责10-15名CRA的日常管理及绩效考核，提升团队监查质量 协调CRO、SMO等供应商，控制项目成本在预算范围内 定期分析项目风险，每月提交2份风险评估报告 任职要求： 临床医学或药学相关专业本科以上学历 2.3年以上CRA管理经验，熟悉ICH-GCP法规 具备2个以上III期临床试验全程管理经验 优秀的跨部门沟通能力，能同时处理5+并行项目
该职位来源于猎聘 1. 熟悉SOP和法规对岗位职责的要求，熟悉所负责的方案及项目文件要求。 2. 能独立完成研究中心管理工作。 3. 有较强的进度和质量的自主管理意识，具备良好的预防及发现风险的能力，对于监查过程中发现的问题可以及时解决或向上反馈。 4. 具备研究中心调研、筛选、启动、监查和中心关闭相关工作的能力，按照要求提交访视报告。 5. 对所负责研究中心进行方案及相关培训，确保研究中心按照方案和适用的法规进行执行研究。 6. 确保研究中心对试验用药品的接收、储存、转运、分发、返还/销毁等流程符合方案、SOP、GCP等法规要求并记录完整、准确。 7. 确保研究中心对试验样本/生物组织的采集
Study Start-Up Clinical Research Associate I ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developm
赛纽仕医药咨询(上海)有限公司该职位来源于猎聘 FSP global Biotech 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. Use
Study Start-Up Clinical Research Associate I ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developm
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Trainee Clinical Research Associate (CRA) – 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
该职位来源于猎聘 Job Responsibilities： - 参与临床试验中心的筛选、评估和调研，协助完成中心资质审核及启动前的准备工作，包括伦理递交、合同签署、中心启动会召开等。 - 按照项目计划和SOP要求，定期对临床试验中心进行现场监查访视，核对原始数据（SDV），确保试验数据真实、完整、可溯源，符合GCP及试验方案要求。 - 负责临床试验中心研究者文件夹（ISF）及受试者资料的日常维护、整理与归档，确保所有文件齐全、规范、及时更新。 - 协助研究者及时上报严重不良事件（SAE）及其他安全性信息，跟踪处理进展，确保符合法规及伦理要求。 - 作为申办方/CRO与研究中心的主要联络人，保
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, clea
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description 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
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 needed to
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description 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
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description 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
该职位来源于猎聘 The Role Become familiar with ICON’s SOPs/WPs, ICH GCP guidelines, appropriate regulations, ICON systems and the principles of and assist with investigator recruitment Maintain timelines and ensure accuracy and completeness of data entered into ICON systems Serve as the primary in-house con
¥82,000 – ¥130,000/año
估算置信度：Low
Estimate based on market data for Shanghai. Actual salaries may vary depending on experience, company, and area.
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