[Hiring] Analytical Monitor @ICON plc

Role Description

As an Advanced Analytical Monitor, you will work across multiple mid to high-complexity studies, delivering deep analytical insights, supporting innovation, and collaborating closely with global cross-functional partners across Data Management, Central Monitoring, and Site Management. You will also provide mentorship to junior colleagues, contributing to the growth and excellence of the wider team.

• Performing analytical monitoring activities for assigned clinical trials, ensuring early identification of site- and subject-level risks, trends, and data quality issues.
• Conducting regular, fit-for-purpose site/subject-level data reviews to detect early warning signals and prevent issue recurrence.
• Accessing and analysing data from multiple systems, reporting tools, platforms, and databases 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.
• Ensuring all activities are conducted in full compliance with relevant SOPs, ICH-GCP requirements, regulatory standards, and project timelines.
• Communicating effectively across multiple stakeholders, managing parallel workstreams, and escalating issues through established pathways.
• Providing training, guidance, and mentoring to junior Analytical Monitors to support capability development across the team.

Qualifications

• Bachelor’s degree in Health Sciences, Data Sciences, or a related discipline; a Master’s degree is preferred.
• Approximately 4+ years of experience within the Pharmaceutical, Biotech, or CRO industry.
• Strong understanding of clinical trial operations, study execution, and data flow within clinical research.
• Demonstrated experience in data analysis within a clinical research environment, including familiarity with core statistical concepts.
• Project, issue, and risk management experience, with the ability to apply critical thinking to drive solutions and support decision-making.
• Experience working with technology platforms and systems used for clinical data collection, analysis, and reporting.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively across global cross-functional teams.
• Strong organisational skills, with the ability to manage multiple priorities in a fast-paced environment.
• Excellent verbal and written communication skills in English.

Requirements

• Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

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.
• Benefits may vary depending on role and location.