scra

Senior Clinical Research AssociateICON 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...

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�...

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....

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....

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...

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...

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....

ICON-Clinical Research Associate II/ SCRA- JR158337ICON 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,...

工作职责1.协助项目经理对公司委托研究的临床项目,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�...

工作职责1.协助项目经理对公司委托研究的临床项目,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�...

该职位来源于猎聘 此岗位为外派Biotech，要求4年及以上CRA经验，优先Car-t 或血液肿瘤背景 主要负责Car-t肿瘤项目，协助PM进行项目及供应商管理等工作 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...

该职位来源于猎聘 在LM的领导下，确保临床研究相关工作严格按照GCP及中国/当地相关法规、临床试验方案、标准操作程序执行。 主要职责： 1.协助项目经理完成研究文件的准备...

该职位来源于猎聘...

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 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 Syneos FSP 外资 Global Biotech 主要负责Oncology项目 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...

该职位来源于猎聘 职责描述： 1. 根据试验方案、合同规定的工作范围、SOP和GCP的要求进行研究中心筛选、启动、监查和关闭访视。 2....