Analytical Monitor
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Analytical Monitor
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Global drug and device development services
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 (Advanced Level) to join our dynamic and expanding client-dedicated Integrated Data Analytics & Reporting team. In this role, you will play a pivotal part in enabling proactive, data-driven risk identification at both site and subject level, directly supporting clinical trial integrity, patient safety, and operational efficiency.
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.
What you will be doing
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.
Your profile
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.
Strong organisational skills, with the ability to manage multiple priorities in a fast-paced environment.
Excellent verbal and written communication skills in English.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.
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