Data Risk Analyst (Remote) – Buenos Aires, Argentina | ICON Strategic Solutions (FSP) Careers 2026
If you're looking to build a rewarding career in clinical
research, data analytics, and healthcare risk management, the Data Risk
Analyst opportunity at ICON Strategic Solutions (FSP) offers an
excellent chance to work remotely while contributing to global clinical trials.
This role is ideal for professionals with experience in clinical data
management, statistics, life sciences, and risk assessment who are
passionate about improving data quality and ensuring regulatory compliance.
Working as a Clinical Data Risk Analyst means becoming part of one of the world's leading healthcare intelligence and clinical research organizations. You will help identify potential risks in clinical trial data, improve data integrity, and support successful drug development programs that ultimately improve patient outcomes worldwide.
Whether you're an experienced clinical data professional or
looking to advance your career in clinical research analytics, this position
provides outstanding learning opportunities, career growth, and exposure to
international research projects.
Job Overview
Job Title: Data Risk Analyst
Company: ICON Strategic Solutions (FSP)
Job ID: JR153437
Department: Clinical Data Management
Location: Buenos Aires, Argentina
Work Mode: Remote
Industry: Clinical Research | Healthcare |
Pharmaceutical | Biotechnology
About the Company
ICON Strategic Solutions (FSP) is part of ICON plc, a
globally recognized healthcare intelligence and clinical research organization
that supports pharmaceutical, biotechnology, and medical device companies
throughout every stage of clinical development.
The organization focuses on innovation, scientific
excellence, regulatory compliance, and patient safety while creating an
inclusive work environment where employees can develop professionally and
contribute to life-changing healthcare solutions.
Professionals joining ICON gain exposure to international
clinical trials, advanced technologies, and multidisciplinary teams working on
some of the most important healthcare projects around the world.
Data Risk Analyst Job Responsibilities
As a Clinical Data Risk Analyst, your primary objective is
to identify, assess, monitor, and reduce risks associated with clinical trial
data throughout the research lifecycle.
Your daily responsibilities may include:
- Conduct
clinical data risk assessments across multiple studies.
- Identify
inconsistencies, missing data, and potential quality issues.
- Recommend
mitigation strategies for identified risks.
- Develop
and support risk management plans.
- Monitor
clinical trial data quality continuously.
- Analyze
datasets using statistical methods.
- Generate
reports and dashboards for stakeholders.
- Collaborate
with Clinical Data Management teams.
- Work
with clinical operations, biostatistics, and regulatory teams.
- Prepare
documentation for inspections and regulatory audits.
- Ensure
compliance with global regulatory standards.
- Support
process improvements for data quality management.
- Communicate
analytical findings clearly to project teams.
- Assist
with risk-based monitoring initiatives.
Required Qualifications
Candidates should ideally possess:
- Bachelor's
degree in Statistics
- Life
Sciences degree
- Biostatistics
- Public
Health
- Pharmacy
- Biotechnology
- Biomedical
Sciences
- Clinical
Research
- Or a
related scientific discipline
Professional experience should include:
- Clinical
Data Management
- Clinical
research
- Risk
assessment
- Healthcare
analytics
- Data
quality management
- Statistical
analysis
- Regulatory
compliance
Required Skills
Successful candidates should demonstrate strong abilities
in:
- Clinical
Data Analysis
- Risk
Assessment
- Data
Validation
- Data
Integrity
- Statistical
Analysis
- Critical
Thinking
- Problem
Solving
- Healthcare
Analytics
- Clinical
Trial Management
- Regulatory
Documentation
- Data
Visualization
- Team
Collaboration
- Communication
Skills
- Attention
to Detail
- Time
Management
Knowledge of statistical software and modern analytical
tools is considered a significant advantage.
Why This Role Is Important
Clinical trials generate enormous volumes of patient and
research data. Any errors or inconsistencies can delay studies, affect
regulatory submissions, or compromise patient safety.
A Data Risk Analyst plays an essential role by identifying
potential issues before they become major problems. Through continuous
monitoring, statistical evaluation, and collaboration with project teams,
analysts help maintain high-quality clinical data and support successful drug
development.
This position directly contributes to:
- Better
patient safety
- Higher
data quality
- Regulatory
compliance
- Faster
clinical trial completion
- Improved
research outcomes
- Reliable
scientific evidence
Benefits of Working at ICON
ICON provides employees with a comprehensive benefits
package designed to support both professional success and personal well-being.
Some highlights include:
- Competitive
salary
- Remote
work opportunity
- Annual
leave benefits
- Health
insurance options
- Retirement
planning programs
- Life
assurance
- Employee
Assistance Programme
- Career
development opportunities
- Global
work environment
- Flexible
country-specific employee benefits
- Inclusive
workplace culture
- Professional
learning resources
- International
career growth opportunities
Career Growth Opportunities
Starting as a Data Risk Analyst can open doors to numerous
advanced positions such as:
- Clinical
Data Manager
- Senior
Data Risk Analyst
- Clinical
Risk Manager
- Risk-Based
Monitoring Specialist
- Clinical
Data Scientist
- Biostatistician
- Data
Quality Manager
- Clinical
Analytics Consultant
- Regulatory
Data Specialist
- Clinical
Operations Manager
With experience, professionals can also transition into
leadership, project management, or global clinical operations roles.
Who Should Apply?
This opportunity is suitable for professionals who enjoy:
- Working
with healthcare data
- Solving
analytical problems
- Clinical
research
- Statistical
analysis
- Data
quality improvement
- Regulatory
compliance
- Remote
collaboration
- Continuous
learning
- International
projects
Fresh graduates with relevant internships and professionals
with clinical research experience are encouraged to explore similar
opportunities within the organization.
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To help job seekers discover this opportunity, the following
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How to Prepare and Practice for This Job
Before applying, invest time in strengthening both your
technical and clinical research knowledge to improve your chances during the
recruitment process.
1. Learn Clinical Research Fundamentals
Understand the phases of clinical trials, Good Clinical
Practice (GCP), patient safety, informed consent, and regulatory requirements.
2. Improve Statistical Knowledge
Practice descriptive statistics, probability, hypothesis
testing, confidence intervals, regression analysis, and data interpretation.
3. Build Data Analysis Skills
Gain hands-on experience using Excel, SQL, R, Python, SAS,
or other statistical software commonly used in healthcare analytics.
4. Understand Clinical Data Management
Study concepts such as:
- Data
cleaning
- Query
management
- Data
validation
- Electronic
Data Capture (EDC)
- Data
reconciliation
- Database
lock process
5. Learn Risk Assessment Techniques
Understand how organizations identify, evaluate, prioritize,
and mitigate risks within clinical studies.
6. Practice Data Visualization
Learn to create clear dashboards and reports using Power BI,
Tableau, or Excel charts that communicate analytical findings effectively.
7. Strengthen Communication Skills
Clinical analysts regularly explain complex findings to
cross-functional teams. Practice presenting technical information in a simple,
business-friendly manner.
8. Prepare for Interview Questions
Expect questions such as:
- Explain
data integrity.
- How
would you identify data quality issues?
- Describe
a clinical data management workflow.
- What
statistical tools have you used?
- How
do you prioritize multiple risks?
- Tell
us about a challenging analytical problem you solved.
9. Review Regulatory Guidelines
Become familiar with international standards such as:
- Good
Clinical Practice (GCP)
- ICH
Guidelines
- FDA
regulations
- EMA
guidance
- Clinical
trial documentation standards
10. Keep Learning
Follow healthcare analytics trends, read clinical research
articles, and complete online certifications related to clinical data
management and risk analysis to remain competitive.
Apply for this Job
Interested candidates can apply directly through the
official company careers page:
Apply Here: https://careers.iconplc.com/job/data-risk-analyst-in-argentina-buenos-aires-jid-51509
