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Central Monitor

  1. Bucharest, Belgrade, Johannesburg
JR155432
  1. Clinical Data Management
  2. ICON Strategic Solutions (FSP)
  3. Remote

About the role

Central Monitor - Hands on CluePoints systems experience required

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.

As a Central Monitor at ICON, you will ensure the quality and integrity of clinical trial data through centralized monitoring activities, contributing to the advancement of innovative treatments and therapies.


What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

  • Conduct remote review and analysis of clinical trial data to identify trends, anomalies, and potential risks to patient safety and data quality.
  • Collaborate with site personnel and clinical teams to address findings from centralized monitoring activities and implement corrective and preventive actions as necessary.
  • Utilize advanced data analytics tools and technology platforms to enhance the efficiency and effectiveness of centralized monitoring processes.
  • Provide support and guidance to study teams on centralized monitoring methodologies, best practices, and regulatory requirements.
  • Contribute to the development and optimization of centralized monitoring strategies and protocols to maximize data quality and compliance across clinical trials.

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

  • Bachelor's degree in life sciences, computer science, or a related discipline
  • Previous experience in clinical research, data management, or monitoring within the pharmaceutical, biotechnology, or CRO industry.
  • Strong understanding of clinical trial processes, regulations, and guidelines (e.g., ICH GCP, FDA regulations).
  • Excellent analytical and critical thinking skills with the ability to identify patterns, trends, and discrepancies in clinical trial data.
  • Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and communicate complex concepts to diverse stakeholders.
  • Willingness to travel as required (approximately 5%)

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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