Social network you want to login/join with:
Site Research Assistant - Cona Ferrara, Ferraracol-narrow-left
Client:IQVIA
Location:Job Category:Other
-
EU work permit required:Yes
col-narrow-right
Job Reference:322373f7d82a
Job Views:4
Posted:
Expiry Date:
col-wide
Job Description:Are you looking for an opportunity to work with an industry-leading company?
IQVIA is currently recruiting for a Site Research Assistant to support a site in Cona, Ferrara.
This role is for 24-40 hours per week and is expected to last approximately 5-6 months.
The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:
Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documentsPlanning and coordinating logistical activity for study procedures according to the study protocolData entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completenessAssisting in study enrollment by recruiting, screening, and orienting volunteers according to the study protocolCorrecting custody of study drug according to site standard operating proceduresCoordinating with study monitor on study issues and effectively responding to monitor-initiated questionsWe are looking for candidates with:
BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g.
clinical research coordinator, Research Assistant, nurse, medical assistant, other medical professionGood knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedulesBasic knowledge of medical terminologyStrong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and WordExcellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clientsGood organizational skills with the ability to pay close attention to detailFluent Italian speaker with good English language skillsIf this sounds like the perfect opportunity for you, please apply now
#LI-CES
#LI-HCPN
#LI-DNP
#LI-NS1
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
Learn more at
#J-18808-Ljbffr