ICON
Analytical Monitor
Mexico · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerICON
- LocationMexico
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
Mexico. Remote - 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.
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What you will be doing
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 (fit-for-purpose) 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.
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.
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.
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:
- 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.
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
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At a glance
- Employment typeFull time
- Employer posted
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Skills in this posting
Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.