🛠️ Launch Your Clinical Tech Career: Configuration & QC Specialist I
Join ICON plc as a Configuration & QC Specialist I and become the quality guardian of clinical trial data systems. This foundational role positions you at the intersection of technology and clinical research, where you'll ensure the accuracy, reliability, and compliance of electronic data capture systems that power groundbreaking medical studies.
As a world-leading healthcare intelligence organization, we're seeking a detail-oriented professional to support the configuration and quality control of clinical trial databases. If you're passionate about data accuracy, enjoy systematic problem-solving, and want to launch your career in clinical technology, this is your opportunity to grow with a global leader while ensuring the integrity of life-changing research data.
🎯 Your Quality Assurance Mission: Key Responsibilities
Clinical Database Configuration Support
- Assist in the configuration and setup of clinical trial databases and electronic data capture (EDC) systems
- Ensure all configurations adhere precisely to project specifications and protocol requirements
- Support the development and implementation of validation plans for EDC system functionality
- Learn and apply clinical data management standards and best practices
Quality Control Excellence
- Perform meticulous quality control checks on clinical trial data and study documentation
- Identify discrepancies, inconsistencies, and data entry errors through systematic review processes
- Document QC findings clearly and support resolution of identified issues
- Participate in data validation activities to ensure reliability throughout the data lifecycle
Cross-Functional Collaboration
- Collaborate with data management, biostatistics, and clinical operations teams to address QC findings
- Support the implementation of corrective and preventive actions for data quality issues
- Work effectively in team-oriented environment to ensure data integrity and regulatory compliance
- Communicate findings and recommendations clearly to technical and clinical team members
Training & Process Support
- Provide support to end-users on system configuration, data entry guidelines, and QC processes
- Assist in developing training materials and user guides for clinical data systems
- Promote compliance and efficiency through clear guidance and support to study teams
- Contribute to process improvement initiatives for enhanced data quality
⭐ Your Profile: Quality & Configuration Fundamentals
Essential Qualifications
- Bachelor's degree in Life Sciences, Computer Science, Health Informatics, or related field
- 1+ years experience in clinical data management, data entry, or related role preferred
- Basic familiarity with clinical trial databases and electronic data capture systems
- Understanding of clinical research processes and data management principles
Technical Foundation
- Interest in clinical data systems such as Medidata Rave, Oracle Clinical, or Inform
- Basic understanding of database concepts and data validation principles
- Familiarity with quality control methodologies and documentation practices
- Willingness to learn evolving technologies and clinical data standards
Professional Attributes
- Exceptional Attention to Detail: Meticulous approach to data accuracy and quality
- Strong Analytical Skills: Ability to identify patterns and discrepancies in complex data
- Excellent Communication: Effective collaboration in team-oriented environment
- Proactive Learning Attitude: Enthusiasm for developing new skills and adapting to processes
Career Launch Qualities
- Eagerness to build expertise in clinical data management and quality assurance
- Ability to follow established procedures while contributing fresh perspectives
- Commitment to accuracy and compliance in regulated environment
- Strong organizational skills for managing multiple tasks and priorities
💫 Why Launch Your Career at ICON?
Foundational Career Opportunity
- Ideal entry point for developing expertise in clinical data management
- Structured training in EDC systems and clinical data quality standards
- Clear pathway to Configuration & QC Specialist II and advanced roles
- Exposure to global clinical research operations and technologies
Professional Development
- Comprehensive onboarding in clinical data management fundamentals
- Mentorship from experienced configuration and quality control professionals
- Opportunities for technical certification and specialized training
- Growth within world-leading clinical research organization
Impact Clinical Research Quality
- Play crucial role in ensuring data integrity for clinical trials
- Contribute to patient safety through accurate data collection systems
- Support regulatory compliance and audit readiness
- Learn industry standards that apply across clinical research
Competitive ICON Benefits
- Attractive entry-level salary package with growth opportunities
- Comprehensive health insurance for you and your family
- Global Employee Assistance Programme with 24/7 support
- Generous annual leave entitlements and flexible scheduling
- Retirement planning benefits from career start
- Professional development allowance and training opportunities
- Supportive team environment with growth-focused culture
📊 Areas You'll Develop Expertise In
- Electronic Data Capture (EDC) System Configuration
- Clinical Data Quality Control Processes
- Database Validation & Testing Methodologies
- Regulatory Compliance Requirements
- Clinical Data Management Standards
🔍 Quality Activities You'll Master
- Data Discrepancy Identification
- Documentation Review & Verification
- System Configuration Validation
- User Acceptance Testing Support
- Process Documentation & Improvement
🎓 Perfect For
- Recent graduates in life sciences or computer science fields
- Professionals with 1-2 years experience seeking clinical research specialization
- Individuals passionate about data quality and regulatory compliance
- Those seeking structured career growth in healthcare technology
✨ Ready to Begin Your Clinical Tech Journey?
If you're a detail-oriented professional with interest in clinical data systems and passion for quality assurance, we encourage you to apply. This Configuration & QC Specialist I role offers the perfect opportunity to launch your career while ensuring the integrity of clinical trial data that advances medical science worldwide.
Apply Now and become ICON's next Clinical Data Quality expert!
