Analytical Monitor

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.

We are currently seeking an Analytical Monitor to join our growing client-dedicated team within Integrated Data Analytics & Reporting. As an Analytical Monitor at ICON, you will play a crucial role in supporting clinical trial oversight through targeted data analytics, early risk identification, and the delivery of high-quality insights that empower Site Managers to make informed, patient-centric decisions.

This is a highly collaborative, analytical role contributing to the overall quality, safety, and operational success of multiple clinical studies across global programmes.

Responsibilities

• Conducting analytical monitoring activities across assigned clinical trials to identify early trends, data quality issues, and potential risks at the site and subject level.
• Performing regular site/subject-level reviews to support proactive issue detection and prevent recurrence.
• Accessing and analysing data from multiple systems, databases, and reporting tools to derive insights that support informed decision-making.
• Collaborating closely with Site Managers, Central Monitoring, and other cross-functional partners to influence site prioritisation and guided risk management.
• Facilitating clear and effective communication with stakeholders, following escalation pathways where appropriate.
• Ensuring all activities are performed in accordance with regulatory guidelines, SOPs, and ICON quality standards.

Your Profile

• Bachelor's degree in Health Sciences, Data Sciences or related field, or equivalent relevant experience.
• Approximately 2+ years of experience within the Pharmaceutical, CRO, Biotech or related industry.
• Strong experience in data analysis and interpretation within a clinical research environment.
• Understanding of clinical trial processes and working knowledge of ICH-GCP and regulatory frameworks.
• Experience with technology platforms and systems used for data collection, analysis, and reporting.
• Strong organisational skills, with the ability to manage multiple priorities in a fast-paced environment.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively across global cross-functional teams.
• Excellent verbal and written communication skills in English.

Rewards & Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways