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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 30000 - 48000 £ 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.
Clinical Research Coordinator / Clinical Research Nurse employer: IQVIA
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 have experience as Clinical Research Coordinators or Nurses. Attend local events or join online forums to connect with individuals who can provide insights and potentially refer you to opportunities at IQVIA.
✨Tip Number 2
Familiarise yourself with the specific therapeutic area of pulmonary/respiratory research. Read up on recent studies, trials, and advancements in this field to demonstrate your knowledge and passion during interviews.
✨Tip Number 3
Prepare to discuss your hands-on clinical experience in detail, particularly your skills in phlebotomy and monitoring vital signs. Be ready to share specific examples of how you've successfully managed patient care and study coordination in previous roles.
✨Tip Number 4
Showcase your IT skills by being proficient in MS Office and any relevant clinical trial management software. Consider taking a short course or certification if you're not fully confident, as this can set you apart from other candidates.
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 specific examples to demonstrate your skills and achievements in these areas.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the role. Mention how your background aligns with the responsibilities outlined in the job description.
Highlight Relevant Skills: In your application, emphasise your IT skills, particularly your proficiency in MS Office. Also, mention your interpersonal and organisational skills, as these are crucial for the role.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is essential 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 respiratory studies.
✨Highlight Relevant Experience
Discuss your hands-on clinical experience, particularly in phlebotomy, ECGs, and vital signs monitoring. Be prepared to provide examples of how you've successfully coordinated study procedures in previous roles.
✨Demonstrate Attention to Detail
Since maintaining accurate study documentation is crucial, be ready to talk about your organisational skills. Mention any systems or methods you use to ensure compliance with protocols and data accuracy.
✨Prepare Questions for the Interviewers
Show your interest in the role by preparing thoughtful questions about the clinical trial processes at IQVIA. This not only demonstrates your knowledge but also your eagerness to contribute to their team.
