THE ROLE
ICON plc is seeking a Senior Clinical Validation Analyst to ensure the accuracy and integrity of clinical trial data through rigorous validation processes. This is a senior position for someone who understands that data quality isn't just about checking boxes—it's about protecting patient safety, enabling regulatory approvals, and bringing new therapies to market.
You will develop validation strategies. You will oversee execution. You will identify issues before they become problems. And you will ensure that when regulators review the data, they find nothing to question.
LOCATION
Flexible / Remote options available
WHY THIS POSITION EXISTS
Clinical trials generate massive amounts of data. Before that data can support regulatory submissions, it must be validated—checked for accuracy, consistency, and compliance with protocols and regulations.
The Senior Clinical Validation Analyst owns this process from end to end. Your work protects the integrity of clinical trials and the patients who depend on them.
WHAT YOU WILL BE DOING
Validation Strategy and Planning
Develop and execute validation strategies and plans for clinical trial data. Ensure validation approaches align with regulatory requirements and internal standards. Design validation protocols that address study-specific needs and risks.
Collaboration and Requirements
Partner with cross-functional teams to identify validation requirements. Work with data managers, biostatisticians, clinical teams, and programmers. Address data quality issues collaboratively and constructively.
Oversight and Analysis
Oversee the review and analysis of validation results. Ensure compliance with regulatory standards and internal protocols. Identify trends and systemic issues requiring broader attention.
Methodology and Improvement
Provide strategic guidance on validation methodologies. Recommend improvements to enhance data reliability. Stay current with evolving validation techniques and tools.
Stakeholder Management
Build and maintain relationships with external partners. Support validation efforts across organizational boundaries. Drive best practices through influence and expertise.
YOUR PROFILE
Education
Advanced degree in life sciences, data science, statistics, or a relevant field.
Experience
Extensive experience in clinical data validation. Strong understanding of regulatory requirements for clinical data. Proven ability to manage complex validation projects effectively.
Technical Skills
Expertise in data analysis and validation tools. Proficiency with relevant software and systems. Understanding of clinical trial data structures and flows.
Professional Competencies
Strong analytical and problem-solving abilities. Excellent communication and interpersonal skills. Stakeholder management and influencing capability. Ability to drive quality improvements in complex organizations.
WHY VALIDATION MATTERS
Regulators don't approve therapies based on trust. They approve based on data.
Every data point in a clinical trial submission has been validated. Someone has checked it. Someone has confirmed it meets standards. Someone has documented the process.
That someone is you.
When a therapy reaches patients, your validation work is part of the reason it's safe. When regulators approve a new drug, your processes helped get it there.
WHAT SUCCESS LOOKS LIKE
In the first 90 days
Understand ICON's validation frameworks and standards. Build relationships with key cross-functional partners. Contribute to validation planning for assigned studies. Demonstrate expertise in validation tools and processes.
In the first year
Lead validation strategy for complex clinical programs. Identify and implement at least one process improvement. Serve as go-to resource for validation questions. Build strong relationships with external partners.
Beyond
Influence validation methodology across the organization. Mentor junior validation team members. Represent ICON in industry discussions on validation best practices. Drive continuous improvement in data quality and reliability.
THE ICON ENVIRONMENT
Global Scale
ICON is a world-leading clinical research organization. You'll work on trials that span countries, therapies, and patient populations.
Collaborative Culture
We work in cross-functional teams. Validation doesn't happen in isolation—it happens in partnership with data managers, programmers, and clinical teams.
Commitment to Quality
Data integrity isn't just a requirement. It's a commitment we make to patients, regulators, and sponsors.
Inclusive Environment
Inclusion and belonging are fundamental to our culture. We value diverse perspectives and the innovation they generate.
Career Development
We invest in our people. There are opportunities to grow, specialize, and take on new challenges.
WHAT ICON OFFERS
Competitive Compensation
Salary and benefits designed to attract and retain top talent.
Annual Leave
Various entitlements to support work-life balance.
Health Insurance
Coverage options for you and your family.
Retirement Planning
Competitive offerings to maximize savings.
Global Employee Assistance
24/7 access to LifeWorks professional support network.
Life Assurance
Protection for your family's financial security.
Flexible Local Benefits
Country-specific options including childcare support, bike schemes, gym discounts, travel subsidies, and health assessments.
QUESTIONS TO ASK YOURSELF
Do I have extensive experience validating clinical trial data?
Can I develop validation strategies that meet regulatory requirements?
Do I work well across functions—with data managers, programmers, and clinical teams?
Am I comfortable influencing without direct authority?
Do I stay current with validation methodologies and tools?
Do I want my expertise to directly support regulatory submissions and patient safety?
APPLICATION PROCESS
Submit your application through the ICON careers portal.
Applications are reviewed by the hiring team.
Qualified candidates are contacted for an initial conversation.
Interviews are conducted with data management leadership and cross-functional partners.
Decisions and offers are communicated in a timely manner.
NOT SURE IF YOU MEET EVERY REQUIREMENT?
Apply anyway.
Studies show that women and underrepresented groups often hesitate to apply unless they check every box. We'd rather hear your story than wonder what we missed. You might be exactly who we're looking for—for this role or another.
READY TO APPLY?
If you're ready to ensure clinical trial data meets the highest standards of accuracy and integrity—and you want to apply your validation expertise at a world-leading CRO—apply now.
Include your resume highlighting validation experience. Add a brief note on your regulatory knowledge and technical expertise. Tell us what interests you about ICON.
Apply for the Senior Clinical Validation Analyst position at ICON plc.
ICON is an equal opportunity employer committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If you need accommodations during the application process, please let us know.
