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- Tasks: Support clinical trials, advocate for patients, and manage study documentation.
- Company: Join IQVIA, a global leader in life sciences, making strides in healthcare innovation.
- Benefits: Part-time hours (24/week), collaborative team environment, and impactful work.
- Why this job: Gain hands-on experience in clinical research while contributing to meaningful healthcare advancements.
- Qualifications: Degree in Life Sciences or equivalent clinical experience; strong IT and interpersonal skills required.
- Other info: Ideal for those with clinical trial experience and a passion for patient care.
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.
Locations
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. Attend local events or join online forums related to clinical trials and respiratory health. This can help you gain insights into the role and potentially connect with someone at IQVIA.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical research, especially those related to pulmonary and respiratory studies. This knowledge will not only boost your confidence but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Prepare for potential interview questions by practising your responses to common scenarios faced by Clinical Research Coordinators. Think about how you would handle patient concerns or manage study documentation effectively.
✨Tip Number 4
Showcase your hands-on clinical experience during discussions. Be ready to share specific examples of your work with phlebotomy, ECGs, or vital signs monitoring, as these are crucial skills for the role at IQVIA.
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 CV and cover letter 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.
✨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 consent forms. Being able to discuss these topics confidently will demonstrate your understanding of the role and your readiness to manage study documentation effectively.
✨Highlight Your Interpersonal Skills
As a Clinical Research Coordinator/Nurse, you'll need excellent interpersonal skills. Prepare to share examples of how you've effectively communicated with patients and team members, ensuring participant safety and addressing concerns.
