A global healthcare leader is seeking a Clinical Research Associate for their operations in Buenos Aires, Argentina.... The role involves managing clinical sites, ensuring compliance with regulations, and developing strong site relationships...
A global healthcare leader is seeking a Clinical Research Associate for their operations in Buenos Aires, Argentina.... The role involves managing clinical sites, ensuring compliance with regulations, and developing strong site relationships...
A global healthcare leader is seeking a Clinical Research Associate for their operations in Buenos Aires, Argentina.... The role involves managing clinical sites, ensuring compliance with regulations, and developing strong site relationships...
. The role involves managing clinical sites, ensuring compliance with regulations, and developing strong site relationships.... Idóneo candidates will have at least 2 years of site management experience in a biopharma environment, be fluent in English...
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance...CRA II ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster...
What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring...Senior CRA ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud...
skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial...Study Start Up CRA 2 ICON plc is a world-leading healthcare intelligence and clinical research organization. We're...
skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial...Study Start Up CRA 2 ICON plc is a world-leading healthcare intelligence and clinical research organization. We're...
where everyone feels like they belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site... at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site...
where everyone feels like they belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site... at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site...
where everyone feels like they belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site... at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site...
where everyone feels like they belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site... at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site...
A global healthcare intelligence organization is seeking a Clinical Research Associate II to manage clinical trials... in Buenos Aires. This role involves conducting monitoring and close-out visits, ensuring data integrity, and collaborating...
. Monitoring site performance metrics and providing regular updates to study teams on site engagement activities and outcomes...Site Engagement Liasion ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re...
all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs..., Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the...
all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs..., Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the...
all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs..., Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the...
all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs..., Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the...
all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs..., Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the...
all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs..., Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the...