đŹ 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.
đŻ 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
â 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
đŤ 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
