Central Monitor

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

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%)

Central Monitoring - Sponsor Dedicated

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

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.

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.