🔬 Advance Medical Breakthroughs Through Clinical Research Excellence
Join ICON plc as a Clinical Research Associate II and become an integral part of our mission to shape the future of clinical development. In this dynamic field-based role, you'll leverage your monitoring expertise to ensure the highest standards of clinical trial execution while contributing to the development of innovative treatments that improve patient lives worldwide.
🎯 Your Impact: Key Responsibilities
Site Management & Monitoring Excellence
- Conduct comprehensive site qualification, initiation, monitoring, and close-out visits
- Serve as primary point of contact for assigned clinical trial sites
- Perform source data verification and ensure data integrity across all study activities
- Develop and implement effective patient recruitment strategies
Quality & Regulatory Compliance
- Ensure strict adherence to ICH-GCP guidelines and regulatory requirements
- Maintain all assigned sites in audit-ready condition
- Monitor patient safety and protocol compliance throughout trial duration
- Review and manage essential study documentation to regulatory standards
Collaborative Partnership
- Build and maintain strong relationships with investigators and site staff
- Collaborate effectively with cross-functional study teams
- Provide expert guidance on site management best practices
- Facilitate clear communication between sites and study management
Study Documentation & Execution
- Contribute to preparation of clinical study reports and protocols
- Manage investigational product accountability and documentation
- Ensure timely data entry and query resolution
- Support regulatory submission preparations as required
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree in Life Sciences, Medicine, or healthcare-related field
- Minimum 2 years of experience as a Clinical Research Associate
- Comprehensive knowledge of ICH-GCP guidelines and clinical trial processes
- Strong organizational skills with excellent attention to detail
- Willingness to travel up to 60% (domestic and international)
- Valid driver's license
Technical Competencies
- Proficiency with Clinical Trial Management Systems (CTMS)
- Experience with electronic data capture systems
- Strong monitoring visit report writing capabilities
- Understanding of regulatory submission requirements
Professional Attributes
- Excellent communication and interpersonal skills
- Strong problem-solving and decision-making abilities
- Ability to work independently and in team environments
- High attention to detail and quality-focused approach
- Adaptability to fast-paced, evolving clinical research landscape
💫 Why Join ICON?
Career Advancement
- Clear pathway to Senior CRA and leadership positions
- Comprehensive training and professional development programs
- Exposure to global clinical trials across multiple therapeutic areas
- Opportunities for specialization in specific disease areas
Meaningful Impact
- Contribute to development of innovative medical treatments
- Ensure patient safety and data integrity in clinical research
- Work with leading pharmaceutical and biotech companies
- Be part of a company dedicated to advancing global health
Comprehensive Benefits
- Competitive compensation package with performance incentives
- Comprehensive health insurance offerings for you and family
- Retirement planning and financial security programs
- Generous vacation entitlements and wellness support
- Global employee assistance program
✨ Ready to Drive Clinical Trial Excellence?
If you're an experienced CRA with a passion for clinical research and a commitment to quality, we encourage you to apply. Join ICON in our mission to accelerate the development of life-changing therapies while advancing your career in clinical research.
Apply Now & Make Your Mark in Clinical Development