IQVIA
ClinicalResearchCoordinator
“Clinical Research Coordinator at IQVIA. Skills: process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement. Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems. Supporting patient screening and enrollment, including handling informed consent and privacy documentation”
What They're Looking For.
Must Have
Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e. g. , clinical research coordinator, research assistant, nurse, medical assistant), Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules, good knowledge of medical terminology, IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access), Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site, Excellent interpersonal and communication skills, organizational skills and attention to detail, Fluency in Italian and good command of English
What You'll Do.
Maintaining and updating study documentation
case report forms (CRFs)
and Electronic Data Capture (EDC) systems
Supporting patient screening and enrollment
including handling informed consent and privacy documentation
Coordinating logistical activities for study procedures in line with the study protocol
Performing data entry
and resolving queries to ensure data accuracy and completeness
Communicating with study monitors and responding to study-related inquiries
Carrying out general administrative tasks related to the study
How You'll Work.
Team & Collaboration
Communicating with study monitors
Communication Scope
Excellent interpersonal and communication skills; Fluency in Italian and good command of English
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