# Analytical Monitor

**Company**: ICON Strategic Solutions
**Work arrangement**: remote
**Experience**: mid
**Job type**: full-time
**Category**: Data Science
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/Analytical-Monitor_JR160486?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_6977c073-5e0

## Description

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

## Skills

### Required
- data analysis
- clinical trial processes
- ICH-GCP
- regulatory frameworks
- organisational skills
- communication skills

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/Analytical-Monitor_JR160486?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)