At a Glance
- Tasks: Ensure quality and integrity of clinical trial data through monitoring and oversight.
- Company: Join ICON plc, a leader in healthcare intelligence and clinical research.
- Benefits: Competitive salary, health insurance, flexible benefits, and global support programmes.
- Why this job: Make a real impact on clinical research while working in an inclusive environment.
- Qualifications: Advanced degree in life sciences and experience in clinical monitoring required.
- Other info: Dynamic team with opportunities for career 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.
- Escalate 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.
Our Benefits
- 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 Strategic Solutions
Contact Detail:
ICON Strategic Solutions 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 researching ICON and its values. Understand their mission and how your skills as a Senior Central Monitor can contribute to shaping the future of clinical development. This will help you stand out during the interview process.
✨Tip Number 3
Practice your communication skills! As a Senior Central Monitor, you'll need to provide clear guidance and support. Mock interviews with friends or mentors can help you articulate your thoughts and experiences effectively.
✨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 genuinely interested in joining our diverse and dynamic team 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 leadership skills you've got. We want to see how you fit into our mission!
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 background aligns with our values at ICON. Keep it concise but impactful – we love a good story!
Showcase Relevant Experience: When filling out your application, be sure to showcase your relevant experience, especially in reviewing Monitoring Visit Reports. We’re looking for specifics, so don’t hold back on the details that demonstrate your expertise.
Apply Through Our Website: We encourage you to apply through our careers site. It’s the best way to ensure your application gets the attention it deserves. Plus, you can explore more about what we offer and our inclusive culture while you’re there!
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trial data and regulatory compliance. Familiarise yourself with the specific responsibilities of a Senior Central Monitor at ICON, as well as any relevant software tools. This will help you answer questions confidently and show that you're genuinely interested in the role.
✨Showcase Your Experience
Prepare to discuss your previous experience in reviewing Monitoring Visit Reports and how you've ensured data quality in past roles. Use specific examples to illustrate your leadership skills and ability to manage multiple projects. This will demonstrate your capability to handle the responsibilities of the position.
✨Ask Insightful Questions
Come prepared with thoughtful questions about the team dynamics, company culture, and how success is measured in the role. This not only shows your interest but also helps you gauge if ICON is the right fit for you. Remember, interviews are a two-way street!
✨Communicate Clearly
Since excellent communication is key for this role, practice articulating your thoughts clearly and concisely. Be ready to explain complex concepts in simple terms, as this will reflect your ability to provide guidance and support to clinical teams effectively.