临床监查员cra-上海 - Shanghai
2周前

工作描述
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
访问所有高级职位,获得理想工作。
类似职位
The Clinical Research Associate will perform monitoring and site management activities for Phase I-IV clinical research projects. · Performs site qualification, site initiation, interim monitoring, and close-out visits. · Maintains a working knowledge of ICH/GCP Guidelines or oth ...
2周前
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. · Performs site qualification, site initiation, interim mo ...
1周前
The Clinical Research Associate will perform monitoring and site management activities for Phase I-IV clinical research projects. · Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits ensuring regulatory compliance. · ...
1个月前
This position is responsible for implementing and monitoring clinical trials to ensure sponsor and investigator obligations are being met. · ...
1周前
Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH GCP guidelines. Assesses the qualification of potential investigative sites, initiates clinical trials at i ...
1周前
The position requires a Clinical Research Associate to verify that human subjects' rights are protected. · The trial data must be accurate, complete, and verifiable from source documents. · The conduct of the trial should comply with GCP and regulatory requirements.Develop collab ...
1周前
The CRA is to verify that the rights and well-being of human subjects are protected. · The reported trial data are accurate, complete, and verifiable from source documents. · The conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP, an ...
2周前
This position is for a Clinical Monitor CRA with a Bachelor's Degree in Life Sciences or an equivalent combination of education, training & experience. Certified Healthcare Professional strongly preferred. · Excellent oral and written communication skills in English. · Ability to ...
4周前
The Clinical Monitoring Associate will be responsible for performing site qualification, site initiation, interim monitoring, site management activities and close-out visits ensuring regulatory compliance. · They will also verify informed consent has been adequately performed and ...
3周前
The Clinical Research Associate 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. · ...
1周前
The Clinical Research Associate 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 or remotely) and to ensure clinical projects are ...
1个月前
The Clinical Research Associate 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. · ...
2周前
The Clinical Research Associate 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 or remotely) and to ensure clinical projects are ...
2周前
The Senior CRA drives study performance at sites. He performs site monitoring activities according to plan in compliance with documents. · He provides monitoring visit reports within timelines. He identifies issues escalates them locally. · He trains supports investigators site s ...
1周前
This is a Senior Clinical Monitor position responsible for implementing and monitoring local clinical trials. · ...
6天前
+Drive study performance at the sites.+Perform site monitoring and other onsite visit activities according to monitoring plan and in compliance with procedural documents.+Provide the required monitoring visit reports within required timelines. Proactively identify study-related i ...
3周前
The Senior Clinical Monitor is responsible for implementing and monitoring local clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH-GCP guidelines. · ...
1个月前
This position involves driving study performance at sites in Taiwan. · Perform site monitoring activities according to monitoring plan. · Provide monitoring visit reports within timelines. · ...
2周前
This position provides early input into protocol design, contracting process focused on data management issues; oversees the process and quality of data management work contracted out to a CRO or research collaborator. · Provides early input into protocol design, contracting proc ...
1个月前
+全日制本科及以上学历 · +具有较强的协调组织及沟通能力, · +能熟练使用常用办公软件, · +接受过系统的临床试验专业知识培训, · +1-3年临床监查工作经验. ...
1个月前
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; · ...
1周前