cra ii - Chengdu

We are seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team.We're proud to foster an inclusive environment driving innovation and excellence. · Monitoring clinical trial sites · Conducting site visits · Collaborating with cross-functional teams ...

The position requires year(s) of experience in tumor project management. · ...

We're seeking a Clinical Research Associate II to join our diverse and dynamic team. · ...

We have successfully supported the top pharmaceutical companies and biotechs across clinical trials. · Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes fai ...

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. · Work Schedule · Standard (Mon-Fri) · Environmental Conditions · Office · Job ...

We are seeking a Clinical Research Associate (Level II) to join our global team. You will have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. · Conduct remote or on-site visits to assess protocol and regulatory compli ...

This position involves performing site qualification, site initiation, interim monitoring, site management activities and close-out visits to ensure regulatory compliance. · The CRA II will use the business card title of Site Management Associate II for Real World Late Phase stud ...

This position is responsible for performing site qualification, site initiation, interim monitoring, site management activities and close-out visits ensuring regulatory compliance. · ...

The Core CRA II is responsible for site management and clinical monitoring activities according to Fortrea's Standard Operating Procedures and ICH GCP Guidelines. · ...

Performs and coordinates different aspects of the clinical monitoring and site management process. · We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. · ...

Performs and coordinates different aspects of the clinical monitoring and site management process. · ...

该职位来源于猎聘 岗位职责: 1、根据SFDA法规,进行临床试验项目管理和质量控制,包括临床试验基地筛选、伦理报批、启动会组织、P沟通、现场访视和质量监控等工作; 2、根据项目计划及进度表,确保项目按计划实施; 3、核查并确保CRF中数据的合法性、准确性和完整性; 4、及时沟通项目经理、申办者和研究者,确保临床试验符合GCP和SDP规范; 5、定期总结和完成项目在医院的监察报告; 6、领导安排的其他工作。 岗位要求: 1、全日制本科及以上学历,临床医学、药学、药理学相关专业; 2、有1.5年以上CRA经验,热爱医药行业,对CRA工作感兴趣; 3、较强团队 ...

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 · Respons ...

· 工作职责 · 能够独立且合格地完成临床试验各流程监查工作并在项目组、直接上级指导下完成各方沟通协调工作。 · 任职要求 · 1、医学或者药学相关专业,本科及以上; · 2、独立且合格地完成临床试验各阶段工作,肿瘤项目相关经验至少1年; · 3、熟悉药物临床试验相关法规,经培训获得 GCP 证书; · 4、掌握临床监查各工作流程及部门各项管理规定,参加相关培训并考核通过; · 5、沟通能力良好,能够适应临床监查的工作环境和工作特点; · 6、工作认真,积极主动,有较好的自主学习能力; · 7、有团队协作意识,团队中反馈良好。 ...

As a Clinical Research Associate (CRA) at Parexel, you will have the opportunity to go beyond the typical clinical monitor role. · ...

该职位来源于猎聘 岗位职责: 1、根据SFDA法规,进行临床试验项目管理和质量控制,包括临床试验基地筛选、伦理报批、启动会组织、Pl沟通、现场访视和质量监控等工作; 2、根据项目计划及进度表,确保项目按计划实施; 3、核查并确保CRF中数据的合法性、准确性和完整性; 4、及时沟通项目经理、申办者和研究者,确保临床试验符合GCP和SDP规范; 5、定期总结和完成项目在医院的监察报告; 6、领导安排的其他工作。 岗位要求: 1、全日制本科及以上学历,临床医学、药学、药理学相关专业; 2、有2年以上CRA经验,热爱医药行业,对CRA工作感兴趣;3、较强团队协作 ...

该职位来源于猎聘 岗位职责:临床试验项目管理和质量控制等工作 岗位要求:全日制本科及以上学历 临床医学相关专业 有CRA经验 · ...

· 工作职责 · 职位描述: · 1、根据GCP和研究方案要求,参与临床试验执行的各个过程,包括试验前可行性评价、伦理递交及合同签署、启动访视、监查访视、关闭研究中心等; · 2、对研究者及CRC进行研究方案、受试者筛选及随访、数据录入和不良反应的处理等培训; · 3、在试验过程中了解研究者对试验方案的执行情况,确认在试验前取得所有受试者的知情同意书,了解受试者的入选率及试验的进展状况,确认入选的受试者合格,协助协调各中心顺利入组; · 4、确认CRC所有数据的记录与报告正确完整,所有病例报告表填写正确,并与原始资料一致。每一受试者的剂量改变、治疗变更 ...

该职位来源于猎聘 职位描述: 1、根据GCP和研究方案要求,参与临床试验执行的各个过程,包括试验前可行性评价、伦理递交及合同签署、启动访视、监查访视、关闭研究中心等; 2、对研究者及CRC进行研究方案、受试者筛选及随访数据录入和不良反应处理等培训; 3、中了解研究者对试验方案的执行情况;确认在试验前取得所有受试者的知情同意书;了解受试者的入选率及进展状况確認合格协助协调顺利入组每一受試者的剂量改变治疗变更合并用药间发疾病失訪情况均應確認並記錄检查遺漏項目提醒researcher補做确认所有不良事件已记录; · 临床医学药学相关专业统招本科以上学历; · ...

Essential Functions · • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. · ...