At a Glance
- Tasks: Support clinical research studies and ensure participant safety while managing data and logistics.
- Company: Join IQVIA, a leader in the clinical research industry.
- Benefits: Gain valuable experience in a dynamic field with flexible hours.
- Other info: Short-term assignment with opportunities for growth in clinical research.
- Why this job: Make a real difference in clinical trials and patient care.
- Qualifications: BS/BA in life sciences or relevant experience in a clinical setting.
The predicted salary is between 30000 - 40000 € per year.
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company? If so, come and join us. IQVIA is currently looking for a Clinical Research Coordinator to support a short-term clinical study.
This is a short-term study assignment (3 months), working 24 hours per week, supporting a site in Hounslow, West London.
As a pivotal member of the site team, you will be involved in a variety of clinical and administrative tasks to support investigators, ensure the smooth running of clinical trials, and assist with the collection of patient data.
Key Responsibilities:- Support clinical research studies and maintain a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.
- Safeguard the well-being of study participants, act as a patient advocate, and address participant concerns.
- Maintain up-to-date study documentation, including study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other essential records.
- Plan and coordinate logistical activities for study procedures in line with the study protocol.
- Perform clinical study set-up and preparation, including labeling specimen collection tubes and containers, managing inventory of required supplies, and setting up or troubleshooting study equipment.
- Assist with data entry, data quality checks, and query resolution to ensure protocol compliance and data accuracy.
- Support study enrollment activities, including recruiting, screening, and orienting participants according to the study protocol.
- Ensure correct custody and handling of study medication in accordance with site standard operating procedures.
- Coordinate with study monitors on study-related issues and respond effectively to monitor-initiated queries.
- Perform and document patient vital signs.
- BS/BA in life sciences or equivalent education and/or relevant work experience in a clinical or medical setting (e.g., Clinical Research Coordinator, Research Nurse, Medical Assistant, or similar role).
- Ideally an experienced Research Nurse or a highly experienced Clinical Research Coordinator.
- Experience in pediatric and/or ophthalmology clinical trials is preferred but not essential.
- Strong knowledge of clinical trials, including departmental, protocol-specific, and study-specific operating procedures, consent forms, and study schedules.
- Strong IT skills, with proficiency in MS Windows and Microsoft Office applications (Access, Outlook, Excel, Word).
- Excellent interpersonal skills with the ability to build and maintain effective working relationships with colleagues, managers, and clients.
- Strong organizational skills with close attention to detail.
Clinical Research Coordinator - London employer: IQVIA Argentina
At IQVIA, we pride ourselves on being an industry leader in clinical research, offering a dynamic work environment that fosters collaboration and innovation. Our London-based team enjoys flexible working hours, a supportive culture that prioritises employee well-being, and ample opportunities for professional growth within the healthcare sector. Join us to make a meaningful impact on patient care while advancing your career in a vibrant city.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Coordinator - London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching the company and understanding their recent projects. Tailor your answers to highlight how your skills align with their needs, especially in clinical trials and patient advocacy.
✨Tip Number 3
Showcase your organisational skills! During interviews, share examples of how you've managed multiple tasks or coordinated logistics in previous roles. This will demonstrate your ability to handle the responsibilities of a Clinical Research Coordinator.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Clinical Research Coordinator - London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Coordinator role. Highlight relevant experience, especially in clinical trials or similar settings. 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 you can contribute to our team. Keep it concise but engaging – we love a good story!
Show Off Your Skills:Don’t forget to showcase your IT skills and any experience with data management systems. Mention specific software you’re familiar with, as this will help us see how you can hit the ground running in the role.
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. We can’t wait to hear from you!
How to prepare for a job interview at IQVIA Argentina
✨Know Your Stuff
Make sure you brush up on clinical research basics and the specific responsibilities of a Clinical Research Coordinator. Familiarise yourself with common protocols, case report forms, and data management systems. This will show that you're not just interested in the role but also understand what it entails.
✨Showcase Your Experience
Be ready to discuss your previous roles in clinical settings, especially if you've worked as a Research Nurse or Clinical Research Coordinator. Highlight any relevant experience with pediatric or ophthalmology trials, even if it's minimal. Real-life examples can make a big impact!
✨Ask Smart Questions
Prepare thoughtful questions about the study you'll be supporting and the team dynamics. This shows your genuine interest in the position and helps you gauge if the company culture aligns with your values. Plus, it gives you a chance to demonstrate your critical thinking skills.
✨Demonstrate Your Interpersonal Skills
Since this role involves working closely with participants and colleagues, be prepared to showcase your interpersonal skills. Share examples of how you've built relationships in past roles and how you handle participant concerns. A friendly, approachable attitude can go a long way!
