Analytical Monitor

ICON Strategic Solutions; México; Remote; MXN 480,000 - 720,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee Assistance Programme (LifeWo​

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions in Mexico offers a sponsor-dedicated model with global expertise. The Analytical Monitor (Advanced Level) will enable proactive, data-driven risk identification at both site and subject levels, 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

Qualifications

• Experience in data analysis within a clinical research environment.
• Excellent communication and collaboration across global cross-functional teams.
• Strong understanding of clinical trial operations and data flow.

Responsibilities

• Perform analytical monitoring to identify site- and subject-level risks, data quality issues, and trends.
• Conduct regular data reviews to detect early warning signals and prevent issue recurrence.
• Access and analyze data from multiple systems to derive actionable insights for decision-making.
• Collaborate with Site Managers, Central Monitoring, and other teams to influence risk management and site prioritization.
• Ensure all activities comply with SOPs, ICH-GCP, regulatory standards, and timelines.
• Communicate effectively across stakeholders and manage parallel workstreams.
• Provide training and mentorship to junior Analytical Monitors.

Skills

Advanced analytical monitoring

Data analysis

Clinical trial operations

Communication

Risk management

Education

Bachelor’s degree in Health Sciences, Data Sciences, or related discipline

Master’s degree preferred

Job description

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.

Analytical Monitor (Advanced Level)

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.

What ICON Can Offer You

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80 000 independent specialized professionals who are there to support you and your family's well‑being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We are dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here