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- Tasks: Support clinical trials and ensure smooth operations while collecting patient data.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Flexible part-time hours, gain valuable experience in the medical field.
- Why this job: Make a real difference in patient outcomes while developing your skills.
- Qualifications: BS/BA in life sciences or relevant experience in a clinical setting.
- Other info: Dynamic team environment with opportunities for growth and learning.
The predicted salary is between 15 - 20 £ per hour.
This part-time (24 hours) role is to support a site in Belfast in conducting a clinical trial in the field of respiratory. As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
Day to day responsibilities will include:
- Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
- Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
- Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
- Plan and coordinate logistical activity for study procedures according to the study protocol
- Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
- Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
- Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
- Correct custody of study drug according to site standard operating procedures
- Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
We are looking for candidates with the following skills and experience:
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
- Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
- Basic knowledge of medical terminology
- Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
- Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
- Good organizational skills with the ability to pay close attention to detail.
Clinical Research Coordinator - Belfast, UK employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator - Belfast, UK
✨Tip Number 1
Network like a pro! Reach out to people in the clinical research field, especially those already working at IQVIA. A friendly chat can open doors and give you insider info about the role.
✨Tip Number 2
Prepare for your interview by brushing up on your knowledge of clinical trials and medical terminology. We want to see that you’re not just passionate but also knowledgeable about the industry!
✨Tip Number 3
Show off your organisational skills! During interviews, share examples of how you've managed multiple tasks or projects. This will highlight your ability to keep things running smoothly in a clinical setting.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining our team at IQVIA.
We think you need these skills to ace Clinical Research Coordinator - Belfast, UK
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Coordinator role. Highlight relevant experience in clinical settings and any specific skills that match the job description. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your skills can contribute to our team in Belfast. Keep it engaging and personal – we love a good story!
Showcase Your Attention to Detail: In clinical research, attention to detail is key. Make sure your application is free from typos and errors. We appreciate candidates who take the time to present their best work, so double-check everything before hitting send!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, you’ll get to explore more about our company and culture while you’re at it!
How to prepare for a job interview at IQVIA LLC
✨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trials, especially in the respiratory field. Familiarise yourself with common protocols and procedures, as well as any recent advancements in the area. This will show your genuine interest and help you answer questions confidently.
✨Showcase Your Interpersonal Skills
As a Clinical Research Coordinator, you'll need to interact with various stakeholders, including patients and investigators. Prepare examples of how you've effectively communicated or resolved issues in past roles. This will demonstrate your ability to build relationships and advocate for volunteers.
✨Be Organised and Detail-Oriented
Highlight your organisational skills during the interview. You might be asked about how you manage multiple tasks or ensure data accuracy. Share specific strategies you use to stay organised, such as using checklists or project management tools, to illustrate your attention to detail.
✨Prepare for Technical Questions
Expect questions related to IT competence, especially regarding MS Office applications. Brush up on your skills in Excel and Access, as you may be asked to discuss how you would handle data entry or quality checking. Being able to talk through your technical abilities will set you apart.
