Drive clinical trial excellence and patient safety. ICON is seeking an experienced Clinical Research Associate II (CRA II) to join our global team. In this pivotal monitoring role, you will be the frontline expert ensuring protocol compliance and data integrity at clinical trial sites. With at least 60% travel, you'll collaborate directly with investigators to advance innovative treatments and contribute to the future of clinical development.
Key Responsibilities
You will be responsible for end-to-end site management and monitoring activities across clinical trial phases.
Site Management & Monitoring:
- Conduct comprehensive site visits (qualification, initiation, monitoring, close-out) to ensure protocol and regulatory compliance
- Perform source data verification and case report form review to maintain data integrity
- Collaborate with investigators and site staff to optimize study conduct and patient safety
Compliance & Documentation:
- Ensure all site activities adhere to ICH-GCP guidelines and regulatory requirements
- Contribute to essential study documentation including protocols and clinical study reports
- Resolve data queries and support site regulatory submissions
Qualifications & Experience
Essential Requirements:
- Bachelor's degree in Life Sciences or healthcare-related field
- Minimum 2 years of independent monitoring experience as a Clinical Research Associate
- Comprehensive knowledge of ICH-GCP guidelines and clinical trial regulations
- Ability to travel 60% (domestic/international) with valid driver's license
Required Skills:
- Exceptional attention to detail and organizational capabilities
- Strong communication and collaboration skills
- Ability to work independently in a fast-paced environment
- Proactive problem-solving approach
Why Join ICON?
Our success depends on our people. When you join ICON, you become part of a team dedicated to excellence in clinical development. We offer:
- Competitive compensation and comprehensive benefits package
- Global Employee Assistance Programme with 24/7 support
- Health insurance and retirement planning options
- Flexible benefits tailored to local markets
- Inclusive culture that values diversity and professional growth
Ready to advance your clinical research career? We encourage you to apply even if you don't meet every requirement. Your unique experience may be exactly what we need.
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