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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 clinical experience required.
- Other info: Ideal for those with hands-on clinical experience and strong IT skills.
The predicted salary is between 30000 - 48000 £ per year.
Join IQVIA as a Clinical Research Coordinator / Clinical Research Nurse (Part-Time – 24 Hours) in Bristol, supporting a respiratory clinical trial.
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.
- 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.
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 work at IQVIA or similar organisations. Attend industry events or webinars to connect with potential colleagues and learn more about the company culture.
✨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 genuine interest in the role during any discussions.
✨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 provide examples of how you've successfully managed patient interactions in previous roles.
✨Tip Number 4
Showcase your IT skills by being proficient in MS Office applications. Consider creating a sample document or spreadsheet that highlights your ability to manage study documentation effectively, as this could impress during interviews.
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 specific experiences that align with the responsibilities listed in the job description. Mention your ability to advocate for patients and ensure their safety.
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 clinical trial protocols. This will show that 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 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 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 will showcase your suitability for the role.
✨Familiarise Yourself with Study Protocols
Before the interview, review common clinical trial protocols and consent forms. Being able to discuss these topics confidently will demonstrate your understanding of the role and its responsibilities.
✨Highlight Your Organisational Skills
Since the role requires maintaining accurate study documentation and coordinating study procedures, be ready to share examples of how you've effectively managed multiple tasks or projects in the past.
