Cra - 398+个职位

该职位来源于猎聘 职责描述： 负责按照分配的项目需求，制定临床试验中心启动计划，定期确认中心进度，确保中心进度符合要求，如有风险，及时采取有效措施或与项目经理沟通调整计划； 协助项目组第三方Vendor人员面试、管理，与项目组成员配合，从而高效合规的推进临床研究工作; 3. 定期检查项目质量，确保负责项目执行质量符合法规，如有违规，需要及时分析和采取措施，必要时与项目经理进行沟通并解决问题; 4. 协助按照分配的项目需求，对Vendor成员进行人员面试、管理，保持和相关供应商的日常评估沟通，督促供应商按计划执行临床项目，并检查执行计划是否有效，是否需要调整; 5. 协助项目团队执行中心选择，负

CRA II/Sr CRA I Syneos 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 th

Thermo Fisher Scientific

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 an Assistant Clinical Research Associate – 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

CRA2 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 development. We are currently seeking a Clinical

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as an Assistant Clinical Research Associate – 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 10

该职位来源于猎聘 职责描述： 负责按照分配的项目需求，制定临床试验中心启动计划，定期确认中心进度，确保中心进度符合要求，如有风险，及时采取有效措施或与项目经理沟通调整计划； 协助项目组第三方Vendor人员面试、管理，与项目组成员配合，从而高效合规的推进临床研究工作; 3. 定期检查项目质量，确保负责项目执行质量符合法规，如有违规，需要及时分析和采取措施，必要时与项目经理进行沟通并解决问题; 4. 协助按照分配的项目需求，对Vendor成员进行人员面试、管理，保持和相关供应商的日常评估沟通，督促供应商按计划执行临床项目，并检查执行计划是否有效，是否需要调整; 5. 协助项目团队执行中心选择，负

Senior CRA, China, office based 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 development We are cu

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

• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of

*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 acr

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as an Assistant Clinical Research Associate – 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

*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

*Job Overview** Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. *Summary Of Responsibilities** Responsible for all aspects

*Updated:** Today *Location:** Beijing, 11, China *Job ID:** 25106905 Not ready to apply? Join our Talent Network *Description** CRA Ⅱ - Beijing/Chengdu Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators a

*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

*Description** CRA Ⅱ - Beijing/Chengdu Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, antic

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

岗位职责: 1. 协助临床监查员开展临床试验项目的现场监查工作，确保试验按照试验方案、GCP原则及相关法规进行。 2. 确保受试者招募和入组计划的顺利进行，及时发现并解决潜在问题。 3. 收集、整理和记录相关资料和数据，确保数据真实、准确、完整。 4. 与研究者、受试者保持良好沟通，及时反馈相关信息。 5. 协助临床项目经理完成其他相关工作。 任职要求: 1. 临床医学、药学、护理学等相关专业在校学生，本科及以上学历。 2. 熟悉临床试验相关法规和GCP原则，具备良好的临床试验基本知识。 3. 具有良好的沟通协调能力和团队合作精神，能够独立工作，也善于与他人合作。 4. 具有责任心和敬业精神。