Clinical Research Coordinator / Clinical Research Nurse

JR United Kingdom; Bath; On-site; GBP 31,000 - 47,000; Part time

Job summary

IQVIA, a leader in life sciences, seeks a part-time Clinical Research Coordinator/Nurse to support respiratory clinical trials in Bristol. Ideal for those with clinical trial experience and skills in patient care and regulatory documentation. Join a collaborative team impacting healthcare innovation.

Qualifications

• Degree in Life Sciences or equivalent clinical experience.
• Proven experience in taking bloods and recording patient vital signs.
• Strong IT skills including proficiency in MS Office.

Responsibilities

• Support the safe conduct of clinical trials under the Principal Investigator.
• Act as a patient advocate ensuring participant safety.
• Coordinate study procedures and maintain accurate documentation.

Skills

Clinical trial coordination

Phlebotomy

Vital signs monitoring

Interpersonal skills

Organizational skills

Education

Degree in Life Sciences

Tools

MS Office

Job description

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Clinical Research Coordinator / Clinical Research Nurse, bath

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Client:

IQVIA

Location:

bath, 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.