CRA(Level II) - Shanghai, Shanghai

+Job summary · This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. · +QualificationsBachelor's degree or equivalent and relevant formal academic / vocational qualification · ...

CRA II, Shanghai, office basedICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical dev ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. · As part of our global team, you'll have the opportunity to perform remote activities on assigned projects in ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, · spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part of our global team,you'll have the opportunity to perform remote activities on assigned · projects in ...

Become familiar with ICON's SOPs/WPs, ICH GCP guidelines and assist with investigator recruitment. · ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. · ...

Assists with remote monitoring and site management activities for clinical trials. · ...

CRA II, Shanghai, office based · ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical ...

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team.We're proud to foster an inclusive environment driving innovation and excellence. · Conducting site qualification · Initiation · Monitoring · Closing visits for clinical trials. · ...

CRA2 · ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · We are curr ...

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advance ...

Site monitoring responsibility for clinical studies according to Company Standard Operating Procedures, · Sponsor Standard Operating Procedures. · Assures the implementation of project plans as assigned. · ...

Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits ensuring regulatory compliance. · ...

This Clinical Monitoring Associate II will be responsible for performing site qualification, · site initiation, interim monitoring, · site management activities and close-out visits (performed on-site or remotely) · ensuring regulatory,IHC-GCP and/or Good Pharmacoepidemiology Pra ...

FSP CRA II is responsible for Description of Responsibilities · A list of all the responsabilities of a FSP CRA II., · The list of pre requisites for this position ...

Clinical research associate responsible for site management and monitoring in clinical studies. Conducts site initiation visits and routine monitoring visits to ensure compliance with ICH GCP guidelines and sponsor requirements. · Site management responsibility for clinical studi ...

Site monitoring and site management responsibility for clinical studies according to Company Standard Operating Procedures Regulatory Guidelines. · ...

Essential Functions · Manage staff in accordance with organization's policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional development, rewarding and disciplining employees, and addres ...

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures,and Regulatory Guidelines. · ...

+Job summary · The job involves performing and coordinating different aspects of the clinical monitoring and site management process. · +ResponsibilitiesMonitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and pro ...