Study Start Up Associate II ICON plc is a world-leading healthcare intelligence and clinical research organization... - Minimum of 1 years’ experience or understanding of clinical study start up requirements and activities. - Knowledge of local...
Study Start Up Associate II ICON plc is a world-leading healthcare intelligence and clinical research organization... of clinical study start up requirements and activities. Knowledge of local and/or international regulatory processes, including...
Study Start Up Associate II ICON plc is a world-leading healthcare intelligence and clinical research organization... or understanding of clinical study start up requirements and activities. Knowledge of local and/or international regulatory processes...
in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study start-up... Where applicable, provide support to Regulatory Affairs Study Start-up Team in the preparation or revision of documentation...
in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study start-up... Where applicable, provide support to Regulatory Affairs Study Start-up Team in the preparation or revision of documentation...
in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study start-up... Where applicable, provide support to Regulatory Affairs Study Start-up Team in the preparation or revision of documentation...
in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study start-up... Where applicable, provide support to Regulatory Affairs Study Start-up Team in the preparation or revision of documentation...
with or oversee study start-up activities, including feasibility, pre-study activities and site selection - Collect, review and track... as per required procedures - Where applicable, provide support to Regulatory Affairs Study Start-up Team in the preparation or revision...
regulatory requirements, SOPs and ICH GCP Assist with or oversee study start-up activities, including feasibility, pre-study... to Regulatory Affairs Study Start-up Team in the preparation or revision of documentation for submission to Ethics Committee...
vendors (CROs and partners) performing data processing, data management and study start-up, study conduct, and study close out... to travel up to 20%**OTHER INFORMATION**None**ORGANIZATIONAL RELATIONSHIPS*** Supports Study and Asset Teams across Research...
vendors (CROs and partners) performing data processing, data management and study start-up, study conduct, and study close out... to travel up to 20%**OTHER INFORMATION**None**ORGANIZATIONAL RELATIONSHIPS*** Supports Study and Asset Teams across Research...
in medium-sized studies, including study start-up and close-out - Knowledge of ICH-GCP guidelines and ability to review... shape an industry. As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment...
the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up... in... Senior Clinical Trial Start-Up Lead $ – $ A leading global clinical research provider is looking for a Senior Study Start...
Oversee vendors (CROs and partners) performing data processing, data management and study start-up, study conduct, and study... to travel up to 20% OTHER INFORMATION None ORGANIZATIONAL RELATIONSHIPS Supports Study and Asset Teams across Research...
for end-to-end project management from start-up through to closeout activities. Tasks & Responsibilities: Services... forecasting. Drive study compliance by maintaining and updating trial management systems, using study tools and management...