FSP CRA(Tianjin) - Beijing

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 a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and r ...

+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 and coordinate all aspects of the clinical ...

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 and coordinate all aspects of the clinical ...

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. · This role involves performing and coordinating all aspects of clinical monitoring · and site management as pa ...

+Perform site management, site administration and site monitoring responsibility for clinical studies according to Fortrea Standard Operating Procedures, ICH Guidelines and GCP. · +Take charge of all aspects of Site Management as prescribed in the project plans.Negotiate study bu ...

Performs and coordinates all aspects of the clinical monitoring and site management process. · Clinical Research Associate conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. · ...

Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. · ...

Perform 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 Practice (GPP) and protocol compliance. · ...

+The Clinical Research Associate II will perform and coordinate all aspects of clinical monitoring and site management process. · +Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to ...

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through r ...

Responsable por la supervisión del sitio clínico según las directrices establecidas por la empresa o patrocinador. · Implementar planes de proyecto asignados. · Mantener archivos estudiando, realizar visitas previas al estudio e iniciación, coordinar con proveedores, entre otros. ...

The CRA I is responsible for site monitoring and management of clinical studies. They ensure the implementation of project plans, perform routine monitoring and closeout of clinical sites, maintain study files, conduct pre-study and initiation visits, liaise with vendors, and oth ...

This position manages clinical studies according to Fortrea Standard Operating Procedures, ICH Guidelines and GCP. · ...

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. · Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sit ...

We are seeking a Clinical Research Associate (Level II) to join our global team. As a CRA, you will perform and coordinate all aspects of clinical monitoring and site management processes. · Conduct remote or on-site visits to assess protocol and regulatory compliance. · Ensure a ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, · Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation · ...

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 conduct remote or on-site visits to assess protocol and regulatory complia ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, · Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation, · As part of our global team,you'll have the opportunity to perform and coordinate ...

We are seeking a Clinical Research Associate (Level II) to perform clinical monitoring tasks in accordance with approved protocols. · Monitors investigator sites with a risk-based monitoring approach. · Evaluates data accuracy through SDR, SDV and CRF review. · ...

We have successfully supported the top 50 pharmaceutical companies.As an Assistant Clinical Research Associate, · you'll provide support with site preparedness, · logistical support to the monitoring process, · and assist with assigned tasks for site management · & remote monitor ...