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Clinical Research Coordinator

Job in Belfast, County Antrim, BT1, Northern Ireland, UK
Listing for: IQVIA
Part Time position
Listed on 2026-01-15
Job specializations:
  • Healthcare
    Clinical Research
Job Description & How to Apply Below

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company that offers you an excellent benefits package and supports career progression whilst giving you the option of working flexibly? If so, come and join us – IQVIA are looking for a Clinical Research Coordinator.

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, ensure the smooth running of clinical trials, and assist with collecting patient data.

Day to day responsibilities
  • 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 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
Qualifications
  • 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 clients
  • Good organizational skills with the ability to pay close attention to detail
Key Skills
  • CSS
  • Cloud Computing
  • Health Education
  • Actuary
  • Building Electrician
Employment Type

Part‑Time

Vacancy

1

Location

Clinical Coordinator
• London, England, UK

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