Scra 职位在 中国

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. · ...

+We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team.+ · +As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol,+regul ...

该职位来源于猎聘 · 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. ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory ...

We are currently 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. · We will contribute to the success of clinical trials by ensuring data integrity, participan ...

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. · Maintain ...

The Clinical Research Associate (CRA) manages and monitors clinical projects according to ICH-GCP, · Standard Operating Procedures (SOP) and local regulatory requirements. · Contribute comments/input in the development of Protocol, Informed Consent Form(ICF), Case Report Forms(CR ...

The role of Sr. CRA I involves performing site qualification, site initiation, interim monitoring, site management and close-out visits to ensure regulatory compliance. · ...

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. · ...

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.Contribute comments/input i ...

The position involves acting as the main line of communication between the sponsor and investigator, verifying research staff qualifications, and ensuring trial safety. · ...

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. · ...

The Senior CRA I is responsible for site monitoring and site management. Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study. Ensure audit readiness at the site level. · Monitor data for ...

The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP and local regulatory requirements. · Contribute comments/input in the development of Protocol, Informed Consent Form (ICF), Case Report Forms (CR ...

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. · ...

The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP. · ...

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. · ...

负责按照分配的项目需求制定临床试验中心启动计划并检查项目质量;协助项目组成员推进临床研究工作;协助按照分配的项目需求对Vendor成员进行人员面试、管理等 · ...

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; · 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; · ...

负责临床试验前、中、后期CRO监查工作, · 协助项目经理组织方案讨论会、中期会、总结会等项目会议工作; · ...