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Clinical Research Coordinator

Job in Belfast, County Antrim, BT1, Northern Ireland, UK
Listing for: IQVIA LLC
Full Time position
Listed on 2025-12-30
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research
Job Description & How to Apply Below
Clinical Research Coordinator - Belfast page is loaded## Clinical Research Coordinator - Belfastlocations:
Belfast, Northern Irelandtime type:
Part time posted on:
Posted Todayjob requisition :
R1509764

This role is to support the site in
** Belfast
* * in conducting a clinical trial for
** 24
* * hours per week.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
** Day to day responsibilities will include:
*** Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
* Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
* Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
* Plan and coordinate logistical activity for study procedures according to the study protocol
* Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
* Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
* Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
* Correct custody of study drug according to site standard operating procedures
* Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
** We are looking for candidates with the following skills and experience:
*** Two years of experience with clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
* 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 client
* Good organizational skills with the ability to pay close attention to detail. #LI-DNP#LI-CES#LI-HCPN#LI-CT1

IQVIA 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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