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- Tasks: Support clinical trials, advocate for patients, and manage study documentation.
- Company: IQVIA is a global leader in life sciences, innovating healthcare solutions.
- Benefits: Part-time hours, collaborative team environment, and impactful work in healthcare.
- Why this job: Join a dynamic team and make a real difference in clinical research.
- Qualifications: Degree in Life Sciences or equivalent experience; phlebotomy and vital signs skills required.
- Other info: This role is part-time (24 hours per week) based in Bristol.
The predicted salary is between 36000 - 60000 £ per year.
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.
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator / Clinical Research Nurse
✨Tip Number 1
Network with professionals in the clinical research field, especially those who work at IQVIA or similar organisations. Attend local events or webinars related to clinical trials and respiratory health to make connections that could lead to job opportunities.
✨Tip Number 2
Familiarise yourself with the latest trends and developments in pulmonary and respiratory clinical trials. This knowledge will not only enhance your understanding but also demonstrate your passion and commitment during interviews.
✨Tip Number 3
Prepare for potential interview questions by practising how you would handle specific scenarios related to patient advocacy and study coordination. Think of examples from your past experience that showcase your skills in these areas.
✨Tip Number 4
Showcase your IT skills by being ready to discuss your proficiency with MS Office and any other relevant software. Consider preparing a brief demonstration of how you've used these tools effectively in previous roles.
We think you need these skills to ace Clinical Research Coordinator / Clinical Research Nurse
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trials, phlebotomy, and patient monitoring. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and outlines your relevant skills and experiences. Mention specific examples of how you've supported clinical trials or worked with patients.
Highlight Relevant Skills: In your application, emphasise your IT skills, particularly your proficiency in MS Office, as well as your understanding of medical terminology and study protocols. This will show you are well-prepared for the role.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in clinical research.
How to prepare for a job interview at IQVIA
✨Show Your Passion for Clinical Research
Make sure to express your enthusiasm for clinical research during the interview. Share specific experiences that highlight your dedication and interest in the field, especially related to pulmonary or respiratory studies.
✨Demonstrate Your Clinical Skills
Be prepared to discuss your hands-on clinical experience, particularly in phlebotomy, ECGs, and vital signs monitoring. Providing examples of how you've successfully performed these tasks in previous roles will showcase your suitability for the position.
✨Familiarise Yourself with Study Protocols
Before the interview, review common clinical trial protocols and understand the key responsibilities of a Clinical Research Coordinator. This knowledge will help you answer questions confidently and demonstrate your readiness for the role.
✨Highlight Your Interpersonal Skills
As a Clinical Research Coordinator, you'll need excellent interpersonal skills. Prepare to discuss how you've effectively communicated with patients and team members in the past, ensuring participant safety and addressing concerns.
