Drive Clinical Excellence and Patient Safety Across Global Trials
At ICON, we don't just conduct clinical research—we shape the future of healthcare. As a world-leading healthcare intelligence and clinical research organization, we're committed to fostering an inclusive environment where innovation and excellence thrive. Join us on our mission to bring life-changing treatments to patients worldwide.
We are seeking a dedicated and detail-oriented Clinical Research Associate II to join our dynamic team. In this role, you'll be the eyes and ears of our clinical trials, ensuring data integrity, patient safety, and regulatory compliance from site initiation to close-out.
Your Impact
As a CRA II at ICON, you'll take ownership of site management activities across multiple countries, building strong relationships with investigators and site staff while ensuring every trial meets the highest standards of quality and compliance.
What You'll Be Doing
🔍 Site Management & Monitoring
- Conduct site qualification, initiation, routine monitoring, and close-out visits across domestic and international locations.
- Ensure protocol compliance, data integrity, and patient safety throughout the entire trial lifecycle.
- Perform source data verification (SDV) and resolve data queries in collaboration with site staff.
🤝 Relationship Building
- Partner with investigators, study coordinators, and site personnel to facilitate seamless study conduct.
- Act as the primary ICON contact for assigned sites, providing guidance and support.
- Identify potential site challenges early and collaborate on solutions.
📋 Documentation & Compliance
- Review and contribute to study documentation, including protocols, monitoring plans, and clinical study reports.
- Ensure all site activities comply with ICH-GCP guidelines, regulatory requirements, and ICON SOPs.
- Maintain accurate, complete, and timely site visit reports and follow-up letters.
📊 Data Integrity
- Perform ongoing data review to maintain high-quality clinical data.
- Track and manage site progress against enrollment targets and milestones.
- Identify trends or issues and escalate appropriately to study teams.
What You'll Bring
Essential Qualifications:
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum 2 years of experience as a Clinical Research Associate in a CRO, pharmaceutical, or biotech environment.
- Deep understanding of clinical trial processes, ICH-GCP guidelines, and global regulatory requirements.
- Proven ability to manage multiple sites and priorities with minimal supervision.
- Strong organizational, communication, and problem-solving skills.
- Willingness to travel up to 60% (domestic and international, fly and drive) with a valid driver's license.
Ideal Attributes:
- Experience in diverse therapeutic areas (oncology, renal, cardiometabolic, etc.).
- Familiarity with electronic data capture (EDC) systems and clinical trial management platforms.
- A proactive, solution-oriented mindset with keen attention to detail.
- Resilient, adaptable, and comfortable working in a fast-paced, matrixed environment.
Why ICON?
Our people are the foundation of our success. We're committed to supporting your well-being, growth, and work-life balance with a comprehensive rewards package.
What We Offer:
- 💰 Competitive Salary – Reflecting your skills, experience, and impact
- 🏖️ Generous Annual Leave – Time to recharge and reset
- 🏥 Comprehensive Health Insurance – For you and your family
- 📈 Retirement Planning – Secure your future with confidence
- 🌍 Global Employee Assistance Programme (LifeWorks) – 24/7 access to professional well-being support
- 🛡️ Life Assurance – Peace of mind for the unexpected
- 🚲 Flexible Local Benefits – May include childcare vouchers, bike schemes, gym discounts, travel subsidies, and more
Inclusion & Belonging
At ICON, inclusion isn't just a policy—it's part of our culture. We provide an accessible, discrimination-free workplace and welcome applications from all qualified candidates. If you require accommodations during the application process, please let us know.
Ready to monitor the trials that shape the future of medicine?
Apply now to join ICON as a Clinical Research Associate II.
