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- Tasks: Ensure quality and integrity of clinical trial data through monitoring and oversight.
- Company: Join ICON plc, a leading healthcare intelligence and clinical research organisation.
- Benefits: Competitive salary, health insurance, flexible benefits, and work-life balance.
- Why this job: Make a real impact in clinical research while fostering innovation and excellence.
- Qualifications: Advanced degree in life sciences and at least 1 year of clinical monitoring experience.
- Other info: Inclusive culture with opportunities for professional growth and development.
The predicted salary is between 36000 - 60000 £ per year.
ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Senior Central Monitor to join our diverse and dynamic team. As a Senior Central Monitor at ICON, you will play a pivotal role in ensuring the quality and integrity of clinical trial data through comprehensive monitoring and oversight. You will be essential in maintaining compliance with regulatory standards, facilitating data accuracy, and supporting the successful execution of clinical research.
What You Will Be Doing:
- Review identified study Monitoring Visit Reports and follow‑up letters from study CRAs, within required timelines.
- Ensure monitoring visit reports and follow‑up letters are documented appropriately according to study parameters, CMP and annotated report.
- Ensure these documents are clear, comprehensive, and detailed.
- Review action items to complete within KPI.
- Provide feedback to CRA on any revisions or additions needed to finalize report.
- Elevate and communicate any concerns or trends to CTM.
- This role will have no interaction with sites, management of sites or management of site data. This role will conduct no site visits.
Your Profile:
- Advanced degree in a relevant field such as life sciences, medicine, or clinical research.
- Must have at least 1 year’s experience reviewing Monitoring Visit Reports.
- Extensive experience in clinical monitoring, with a strong focus on data quality and regulatory compliance.
- Demonstrated leadership skills with the ability to manage multiple projects and collaborate effectively with cross‑functional teams.
- Expertise in data management and analysis, with proficiency in relevant software and monitoring tools.
- Excellent communication and interpersonal skills, with the ability to provide clear guidance and support to clinical teams.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.
- Life assurance
- Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Senior Central Monitor employer: ICON
Contact Detail:
ICON Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Central Monitor
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical trial data integrity and regulatory compliance. We want you to shine, so practice answering common questions and think about how your experience aligns with what ICON is looking for.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email to express your appreciation and reiterate your interest in the role. It shows you’re keen and professional.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, you’ll find all the latest roles and updates directly from us at ICON.
We think you need these skills to ace Senior Central Monitor
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Central Monitor role. Highlight your experience in clinical monitoring and data quality, as well as any relevant software skills. 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 mission at ICON. Keep it concise but impactful – we love a good story!
Showcase Your Leadership Skills: Since this role involves collaboration with cross-functional teams, make sure to highlight your leadership experience. Share examples of how you've managed projects or guided teams in the past. We’re all about teamwork here at ICON!
Apply Through Our Website: Don’t forget to apply through our careers site! It’s the best way to ensure your application gets to us directly. Plus, you can explore more about the benefits we offer and get a feel for our culture.
How to prepare for a job interview at ICON
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trial data and regulatory compliance. Familiarise yourself with the specific monitoring tools and software mentioned in the job description, as this will show that you're serious about the role and understand what’s required.
✨Showcase Your Experience
Prepare to discuss your previous experience in reviewing Monitoring Visit Reports. Have specific examples ready that highlight your attention to detail and how you've ensured data quality in past roles. This will demonstrate your capability to handle the responsibilities of a Senior Central Monitor.
✨Communicate Clearly
Since excellent communication skills are crucial for this role, practice articulating your thoughts clearly and concisely. You might be asked to provide feedback or guidance, so being able to express your ideas effectively will set you apart from other candidates.
✨Emphasise Team Collaboration
Highlight your ability to work with cross-functional teams. Prepare examples of how you've successfully collaborated with others in the past, especially in high-pressure situations. This will show that you can thrive in ICON's diverse and dynamic environment.
