Study Start Up CRA 2 ICON plc is a world-leading healthcare intelligence and clinical research organization. We're... to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate (CRA...
Study Start Up CRA 2 ICON plc is a world-leading healthcare intelligence and clinical research organization. We're... to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate (CRA...
protocols and sites in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct... reports appropriately in a timely manner. Collects, reviews, and monitors required regulatory documentation for study start...
protocols and sites in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct... reports appropriately in a timely manner. Collects, reviews, and monitors required regulatory documentation for study start...
protocols and sites in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct... reports appropriately in a timely manner. Collects, reviews, and monitors required regulatory documentation for study start...
protocols and sites in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct... reports appropriately in a timely manner. Collects, reviews, and monitors required regulatory documentation for study start...
protocols and sites in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct... reports appropriately in a timely manner. Collects, reviews, and monitors required regulatory documentation for study start...
protocols and sites in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct... reports appropriately in a timely manner. Collects, reviews, and monitors required regulatory documentation for study start...
. Interaction with sites/CRA and follow-up on study required milestones from the project start until close out. May act as backup... projects and evaluate the quality and integrity of the study as per the protocol, SOPs, respective regulations and guideline...
activation - Achieves PPD’s target cycle times for site - May work with the start-up CRA(s) to prepare the regulatory... functional departments to ensure various site start-up activities are aligned with submissions activities and mutually agreed...
from start-up through to closeout activities. Tasks & Responsibilities Services rendered will adhere to applicable Sponsor SOPs..., contingency and risk management, and budget forecasting. Drive study compliance by maintaining and updating trial management...
in a timely manner. Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance... in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country...