At a Glance
- Tasks: Support clinical studies and ensure smooth running of trials while advocating for patient well-being.
- Company: Join IQVIA, an industry leader in clinical research with a dynamic team.
- Benefits: Gain valuable experience in clinical research with flexible hours and a supportive environment.
- Other info: Short-term assignment with opportunities for growth in the clinical research field.
- Why this job: Make a real difference in patients' lives while developing your skills in a fast-paced setting.
- Qualifications: BS/BA in life sciences or relevant experience; strong IT and interpersonal skills required.
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 known for its rich history and diverse community.
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 the specific role. Familiarise yourself with their recent projects and values. This will help you tailor your answers and show that you're genuinely interested in the position.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online platforms to get comfortable with common interview questions. The more you practice, the more confident you'll feel when it’s your turn to shine.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you an edge. Plus, it’s super easy to keep track of your applications!
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 any relevant experience in clinical trials, especially if you've worked with pediatric or ophthalmology studies. We want to see how your background fits 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 align with our needs. Be sure to mention your ability to maintain study documentation and support patient well-being.
Show Off Your IT Skills:Since strong IT skills are a must, don’t forget to mention your proficiency in MS Office applications. If you have experience with Electronic Data Capture systems, make that known too! We love tech-savvy candidates.
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. Plus, we love seeing applications come directly from our site!
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
Prepare to discuss your previous roles in clinical settings, especially any experience related to clinical trials. Be ready to share specific examples of how you've supported studies, managed patient data, or coordinated logistics. This will help demonstrate your hands-on knowledge and suitability for the position.
✨Ask Smart Questions
Interviews are a two-way street! Prepare thoughtful questions about the study you'll be working on, the team dynamics, or the company's approach to patient advocacy. This shows your genuine interest in the role and helps you gauge if it's the right fit for you.
✨Be Personable
Since this role involves interacting with patients and colleagues, it's crucial to showcase your interpersonal skills. Practice being friendly and approachable during the interview. A positive attitude can go a long way in making a lasting impression!
