Clinical Research Coordinator / Clinical Research Nurse

JR United Kingdom; Newtownabbey; On-site; GBP 20,000 - 30,000; Part time

Job summary

Join IQVIA as a Clinical Research Coordinator / Nurse, where you'll support respiratory clinical trials in Belfast. This part-time role (24 hours/week) is ideal for someone with hands-on clinical experience, including phlebotomy and study coordination. You will ensure participant safety, maintain accurate documentation, and coordinate study procedures, all while contributing to impactful healthcare advancements.

Qualifications

• Proven experience in taking bloods and recording patient vital signs.
• Familiarity with clinical trial protocols and consent forms.
• Basic understanding of medical terminology.

Responsibilities

• Support the conduct of clinical trials under the guidance of Principal Investigator.
• Maintain accurate study documentation including protocols and CRFs.
• Recruit, screen, and orient study participants.

Skills

Phlebotomy

Vital Signs Monitoring

Study Coordination

Interpersonal Skills

Organizational Skills

Education

Degree in Life Sciences or equivalent clinical experience

Tools

MS Office

Job description

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Clinical Research Coordinator / Clinical Research Nurse, newtownabbey

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Client:

IQVIA

Location:

newtownabbey, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

07.06.2025

Expiry Date:

22.07.2025

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Job Description:

Join IQVIA as a Clinical Research Coordinator / Clinical Research Nurse (Part-Time – 24 Hours)

Location: Belfast | Therapeutic Area: Respiratory

Are you passionate about clinical research and ready to take the next step in your career? IQVIA, a global leader in life sciences, is seeking a dedicated Clinical Research Coordinator / Clinical Research Nurse to support a respiratory clinical trial at a site in Belfast.

This is a part-time role (24 hours per week) ideal for someone with a background in clinical trials and hands-on clinical experience, including phlebotomy, ECGs, vital signs monitoring, and study coordination.

Your Key Responsibilities:

• Support the safe and effective conduct of clinical trials under the guidance of the Principal Investigator.
• Act as a patient advocate, ensuring participant safety and addressing concerns.
• Maintain accurate study documentation including protocols, CRFs, and EDC systems.
• Coordinate and prepare for study procedures, including equipment setup and specimen labelling.
• Assist with data entry, quality checks, and resolution of queries to ensure protocol compliance.
• Recruit, screen, and orient study participants in line with protocol requirements.
• Manage study drug custody in accordance with SOPs.
• Liaise with study monitors and respond to queries effectively.
• What We’re Looking For:
• A degree in Life Sciences or equivalent clinical experience (e.g., nurse, medical assistant).
• Proven experience in taking bloods and recording patient vital signs.
• Familiarity with clinical trial protocols, consent forms, and study schedules.
• Basic understanding of medical terminology.
• Strong IT skills, including proficiency in MS Office (Word, Excel, Outlook, Access).
• Excellent interpersonal and organizational skills with a keen eye for detail.

Why Join IQVIA?

At IQVIA, you’ll be part of a collaborative team that’s driving innovation in clinical research. We offer a supportive environment where your contributions make a real impact on advancing healthcare.