🔍 Advance Clinical Research as a Clinical Research Associate II
Join ICON plc, a world-leading healthcare intelligence and clinical research organization, as a Clinical Research Associate II. In this dynamic role, you'll be at the forefront of clinical trial execution, ensuring data integrity and patient safety while contributing to groundbreaking treatments that shape the future of healthcare.
🎯 Your Impact: Key Responsibilities
Clinical Trial Site Management
- Conduct comprehensive site visits including qualification, initiation, monitoring, and close-out
- Ensure strict protocol compliance and adherence to ICH-GCP guidelines
- Monitor patient safety and verify proper informed consent processes
- Perform source data verification and maintain data integrity standards
Data Quality & Documentation Excellence
- Review clinical data and resolve queries to ensure high-quality dataset completion
- Contribute to preparation and review of essential study documentation
- Maintain accurate and complete trial documentation and monitoring reports
- Support regulatory compliance and inspection readiness at assigned sites
Stakeholder Collaboration & Communication
- Build strong relationships with investigators and site staff
- Collaborate with cross-functional study team members
- Provide training and support to site personnel as needed
- Facilitate smooth study conduct through effective communication
Risk Management & Protocol Adherence
- Identify and address potential issues proactively
- Ensure regulatory compliance at assigned clinical sites
- Monitor site performance and implement corrective actions
- Maintain patient safety and data quality throughout trial lifecycle
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of experience as a Clinical Research Associate
- In-depth knowledge of ICH-GCP guidelines and clinical trial regulations
- Ability to travel approximately 60% (international and domestic)
- Valid driver's license required
Technical Competencies
- Comprehensive understanding of clinical trial processes
- Experience with site management and monitoring procedures
- Knowledge of regulatory requirements and compliance standards
- Proficiency in data review and query resolution processes
Professional Attributes
- Exceptional organizational skills and attention to detail
- Strong verbal and written communication abilities
- Capable of working independently and collaboratively
- Adaptable to fast-paced, dynamic environments
- Excellent problem-solving and critical thinking skills
💫 Why Join ICON plc?
Meaningful Work & Global Impact
- Contribute to groundbreaking clinical research that advances patient care
- Work with a world-leading CRO committed to healthcare innovation
- Play a crucial role in bringing new treatments to patients worldwide
- Join an inclusive environment that values diversity and excellence
Professional Growth & Development
- Clear career progression pathways in clinical research
- Comprehensive training and mentorship programs
- Exposure to diverse therapeutic areas and study phases
- Opportunities for professional certification support
Competitive Compensation & Benefits
- Attractive salary package with performance incentives
- Comprehensive health insurance options for you and your family
- Global Employee Assistance Programme with 24/7 support
- Flexible work arrangements and work-life balance focus
Additional Benefits
- Generous annual leave entitlements
- Competitive retirement planning options
- Life assurance coverage
- Country-specific benefits including:
- Travel passes and transportation benefits
- Gym membership discounts
- Health assessments
- Childcare support programs
✨ Ready to Drive Clinical Trial Excellence?
If you're an experienced CRA with 2+ years of monitoring experience and passion for advancing clinical research, we encourage you to apply. This role offers the perfect opportunity to grow your career while making a meaningful impact on global healthcare development.
Apply Now & Become Our Next Clinical Research Associate II!
