scra

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 Key responsibilities: • Monitors 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 accuracy through SDR, SDV...

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....

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 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 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,...

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�...

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；...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development and technology solutions across more than 20 therapeutic areas. With over 18,000 staff conducting...

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....

该职位来源于猎聘 工作职责： 1、 能独立完成研究中心筛选、临床试验会议、与研究中心伦理、机构的沟通、研究中心启动、常规监查、中心关闭、协助内外部稽查等。 2、 及时与项目经理、申办者和研究者沟通，保证临床试验按照国家GCP要求和试验方案进行。 3、...

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....

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 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；...

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...

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 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 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 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；...