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- Tasks: Ensure the quality and integrity of clinical trial data through monitoring and reporting.
- Company: Leading clinical research organisation in the UK with a focus on innovation.
- Benefits: Competitive benefits and opportunities for professional growth.
- Why this job: Make a real impact in clinical research while advancing your career.
- Qualifications: Advanced degree in a relevant field and experience in clinical monitoring.
- Other info: Join a dynamic team dedicated to improving healthcare outcomes.
The predicted salary is between 36000 - 60000 £ per year.
A leading clinical research organization in the UK is seeking a Senior Central Monitor to ensure the quality and integrity of clinical trial data. The successful candidate will monitor and review reports, ensuring compliance and supporting clinical research execution.
Candidates should have an advanced degree in a relevant field and at least one year's experience in clinical monitoring. Strong communication skills and proficiency in data management tools are essential. This role offers competitive benefits and opportunities for professional growth.
Senior Central Monitor - Data Quality & Compliance employer: ICON
Contact Detail:
ICON Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Central Monitor - Data Quality & Compliance
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Senior Central Monitor role.
✨Tip Number 2
Prepare for interviews by brushing up on your data management tools and compliance knowledge. We recommend practising common interview questions related to clinical monitoring so you can showcase your expertise confidently.
✨Tip Number 3
Don’t just apply anywhere; focus on organisations that align with your values and career goals. We suggest checking out our website for tailored job listings that fit your skills and aspirations in clinical research.
✨Tip Number 4
Follow up after interviews! A simple thank-you email can set you apart from other candidates. We believe it shows your enthusiasm for the role and keeps you fresh in the interviewer’s mind.
We think you need these skills to ace Senior Central Monitor - Data Quality & Compliance
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical monitoring and data management. We want to see how your skills align with the role of Senior Central Monitor, so don’t hold back on showcasing your achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about ensuring data quality and compliance in clinical trials. We love seeing candidates who can communicate their enthusiasm and fit for the role.
Showcase Your Communication Skills: Since strong communication skills are essential for this role, make sure to demonstrate them in your application. Whether it’s through clear language in your CV or cover letter, we want to see that you can convey complex information effectively.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the position. Plus, it’s super easy to do!
How to prepare for a job interview at ICON
✨Know Your Data Inside Out
As a Senior Central Monitor, you'll be dealing with clinical trial data daily. Make sure you brush up on your knowledge of data management tools and the specific compliance standards relevant to clinical research. Being able to discuss these confidently will show your expertise.
✨Showcase Your Communication Skills
Strong communication is key in this role. Prepare examples of how you've effectively communicated complex data findings to different stakeholders in the past. This will demonstrate your ability to convey important information clearly and concisely.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in previous roles related to data quality and compliance, and be ready to explain how you handled them. This will highlight your practical experience.
✨Research the Organisation
Familiarise yourself with the clinical research organisation's mission, values, and recent projects. This knowledge will not only help you tailor your answers but also show your genuine interest in the role and the company. It’s a great way to connect your skills to their needs.
