reimbursements. May build and enter budgets and SVTs;work on transparency reporting;perform study reconciliations;manage...Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Site Payments...
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical... Clinical Trial Coordinator, you'll coordinate and facilitate project activities and may serve as a study lead, acting...
study decisions and outcomes. Providing strategic guidance on data governance, quality control, and compliance... and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave...
, and other ancillary agreements with study sites using critical thinking, available tools/systems/documents, historical data, and adheres... with ICON’s rules, procedures, and policies. Maintains consistent communication with study sites and internal stakeholders...
Site Management Associate (Study Delivery Specialist) ICON plc is a world-leading healthcare intelligence... management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols...
launch issues Work will involve some weekends and travel which may be extensive at times in addition to potential off shift... material movement Develop interfaces, and work with cross functional teams to develop / define common tooling and process...
study documents from templates in the set-up phase of a study, e.g., communication/escalation plan, ICOLABS forms.... Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities...
Study Support Assistant ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re... to shape the future of clinical development We are looking for a Study Support Assistant for the Site Activation department...
requirements. Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory... submissions. Support the preparation of study-related materials, such as informed consent forms and case report forms...
of clinical development We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team. As a Study... stakeholders to obtain necessary approvals and authorizations for study initiation. Managing and maintaining comprehensive...