Clinical Research Coordinator

IQVIA

Belfast

On-site

GBP 25,000 - 35,000

Part time

14 days+

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Job summary

IQVIA is seeking a part-time Clinical Research Coordinator in Belfast to support clinical trials in respiratory health. The role involves administrative tasks, ensuring compliance with study protocols, and maintaining relationships with study participants. Ideal candidates should have a relevant degree and strong organizational skills, with a focus on detail and interpersonal communication.

Qualifications

BS/BA in life sciences or equivalent experience in a clinical environment.
Basic knowledge of clinical trials and medical terminology.
Strong IT skills, proficient in MS Windows and Office applications.

Responsibilities

Support clinical research studies and maintain a safe study environment.
Assist with data entry and ensure adherence to study protocols.
Coordinate with study monitor on study issues.

Skills

Interpersonal skills

Organizational skills

Attention to detail

Basic knowledge of clinical trials

Strong IT competence

Education

BS/BA in life sciences

Tools

MS Office

Job description

IQVIA Belfast, Northern Ireland, United Kingdom

Clinical Research Coordinator

IQVIA Belfast, Northern Ireland, United Kingdom

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Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.

This part-time (24 hours) role is to support a site in Belfast in conducting a clinical trial in the field of respiratory.

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:

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, nurse, medical assistant, other medical profession
Basic knowledge of 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.

Seniority level