Clinical Research Coordinator / Clinical Research Nurse

JR United Kingdom; Newport; On-site; GBP 25,000 - 35,000; Part time

Job summary

A leading company in life sciences seeks a Clinical Research Coordinator / Clinical Research Nurse in Newport for a part-time role in clinical trials. This position involves supporting respiratory clinical trials, ensuring participant safety, and managing study documentation. Ideal candidates will have a clinical background with hands-on experience in taking bloods and documenting vital signs.

Qualifications

• Experience in taking bloods and recording patient vital signs.
• Familiarity with clinical trial protocols, consent forms, and study schedules.
• Basic understanding of medical terminology.

Responsibilities

• Support safe conduct of clinical trials under Principal Investigator guidance.
• Maintain accurate study documentation including protocols and CRFs.
• Recruit, screen, and orient study participants in line with protocol requirements.

Skills

Phlebotomy

ECGs

Vital Signs Monitoring

Study Coordination

Interpersonal Skills

Organizational Skills

Attention to Detail

Education

Degree in Life Sciences or equivalent clinical experience

Tools

MS Office (Word, Excel, Outlook, Access)

Job description

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Clinical Research Coordinator / Clinical Research Nurse, newport, wales

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Client:

IQVIA

Location:

newport, wales, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2

Posted:

06.06.2025

Expiry Date:

21.07.2025

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Job Description:

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

Location: Bristol | Therapeutic Area: Pulmonary/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 Bristol.

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.