Site Research Assistant - Torpoint, Cornwall page is loaded## Site Research Assistant - Torpoint, Cornwalllocations: Cornwall, United Kingdomtime type: Part timeposted on: Posted Todayjob requisition id: R1506060This role with an immediate start is for **24** **hours** per week and is expected to last around one year. Working day will be Friday.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 documents* Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.);* Planning and coordinating logistical activity for study procedures according to the study protocol* Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness* Management and shipment of biological samples* Performing ECG, taking vital signs, phlebotomy* Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions* Administrative research taskWe 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 profession* Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules* **Must have at least 2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial site*** Basic knowledge of medical terminology* Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word* Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients* Good organizational skills with the ability to pay close attention to detailIf this sounds like the perfect opportunity for you, please apply now!#LI-CES#LI-CT1#LI-HCPN#LI-DNPIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more atIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
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