Clinical Research Coordinator / Clinical Research Nurse

JR United Kingdom; Bristol; On-site; GBP 80,000 - 100,000; Part time

Job summary

Join a leading company as a part-time Clinical Research Coordinator / Nurse in Bristol, focusing on respiratory clinical trials. The role involves participant safety, data management, and study oversight in a supportive environment emphasizing healthcare innovation.

Qualifications

• Degree in Life Sciences or equivalent clinical experience.
• Experience in blood sampling and recording vital signs.
• Knowledge of clinical trial protocols and consent forms.

Responsibilities

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

Skills

Attention to detail

Interpersonal skills

Organizational skills

Education

Degree in Life Sciences or equivalent clinical experience

Tools

MS Office

Job description

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

Location:

Bristol | Therapeutic Area: Pulmonary/Respiratory

Job Description:

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) suitable for someone with clinical trial experience, including phlebotomy, ECGs, vital signs monitoring, and study coordination.

Your Key Responsibilities:

1. Support the conduct of clinical trials under the guidance of the Principal Investigator.
2. Ensure participant safety and address concerns as a patient advocate.
3. Maintain accurate study documentation including protocols, CRFs, and EDC systems.
4. Prepare for study procedures, including equipment setup and specimen labelling.
5. Assist with data entry, quality checks, and query resolution to ensure protocol compliance.
6. Recruit, screen, and orient study participants according to protocol.
7. Manage study drug custody following SOPs.
8. Liaise with study monitors and respond to queries effectively.

What We’re Looking For:

1. A degree in Life Sciences or equivalent clinical experience (e.g., nurse, medical assistant).
2. Experience in blood sampling and recording vital signs.
3. Knowledge of clinical trial protocols, consent forms, and study schedules.
4. Understanding of medical terminology.
5. Proficiency in MS Office (Word, Excel, Outlook, Access).
6. Strong interpersonal and organizational skills with attention to detail.

Why Join IQVIA?

Be part of a collaborative team driving innovation in clinical research. We offer a supportive environment where your contributions impact healthcare advancements.