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Sr Central Monitor

  1. Livingston
JR146206
  1. Clinical Monitoring
  2. ICON Strategic Solutions (FSP)
  3. Remote

About the role

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Sr CRA/Central Monitor

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.

Job title - Senior Central Monitor

Location - Must be based in the UK

Fully sponsor dedicated

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.

  • Individual will ensure monitoring visit reports and follow-up letters are documented appropriately according to study parameters, CMP and annotated report.  This person will ensure these documents are clear, comprehensive, and detailed.

  • Review action items to complete within KPI

  • This individual with provide feedback to CRA on any revisions or additions needed to finalize report.

  • This individual will escalate and communicate any concerns or trends to CTM.

  • This role will have no interaction of 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 years' 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 examples include:

  • 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.

Visit our careers site to read more about the benefits ICON offers.

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.

Are you a current ICON Employee? Please click here to apply

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Day in the life

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Suzaita's story - an insight into working in Clinical Research

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Summary

Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfil

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Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

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