Position Overview:
Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance
Summarized Purpose:
Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or onsite visits to assess protocol and regulatory co
The Role:
Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
Submissi
Job Description
Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes fail
Job Description
As a specialist in Supplier Risk Management your main responsibilities will be in designing, configuring and adopting processes for supplier on-boarding and risk assessment.
Wo
As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-o
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-o
As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close
Job Overview
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
Responsibilities
You will be responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites maintenance of study files, conduct of pre-study and ini
Job Overview
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
Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures
Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures
CRA II or Senior CRA
Officebased- Johannesberg/Durban or Homebased
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance
Job Overview
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
Job Overview
Perform monitoring and site management work for a variety of protocols, site and therapeutic areas.
Essential Functions
Perform site monitoring visits (selection, initiation, mo
