Advance Clinical Trials as a Clinical Research Associate II (CRA II) at ICON
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we help accelerate the development of drugs and devices that save lives.
We are looking for a motivated Clinical Research Associate II (CRA II) to join our growing team. In this role, you will be the vital link between ICON and clinical trial sites, ensuring the integrity and progress of groundbreaking clinical studies. If you are an experienced CRA ready to take the next step in your career with a industry leader, we encourage you to apply.
What You Will Do:
As a CRA II, you will be responsible for the end-to-end management and monitoring of clinical trial sites:
- Conduct All Site Visits: Perform site qualification, initiation, monitoring, and close-out visits, ensuring compliance with the protocol and regulatory standards.
- Ensure Data Integrity & Patient Safety: Perform source data verification, review case report forms (eCRF), and resolve data queries to guarantee the highest quality of clinical data.
- Build Key Relationships: Serve as the main point of contact for investigators and site staff, providing training and support to ensure smooth study conduct.
- Maintain Regulatory Compliance: Ensure all site activities adhere to ICH-GCP guidelines, local regulations, and standard operating procedures (SOPs).
- Manage Study Documentation: Contribute to the preparation and review of essential documents, including protocols, informed consent forms, and clinical study reports.
Your Profile & Qualifications:
Required Experience & Skills:
- Bachelor's degree in a Life Science, Nursing, or related healthcare field.
- A minimum of 2 years of experience as a Clinical Research Associate (CRA).
- In-depth knowledge of clinical trial conduct and ICH-GCP guidelines.
- Proven ability to manage multiple sites independently with strong attention to detail.
- Excellent communication, problem-solving, and organizational skills.
- Willingness and ability to travel approximately 60% of the time (domestic and international) and possession of a valid driver’s license.
What ICON Offers You:
Our success depends on our people. We offer a competitive salary and a comprehensive benefits package focused on your well-being and professional growth:
- Competitive Salary & Benefits: A rewarding package with health insurance, retirement planning, and life assurance.
- Work-Life Balance: Flexible benefits including generous annual leave and family-focused support.
- Supportive Environment: Access to our Global Employee Assistance Programme for you and your family.
- Career Growth: Clear paths for professional development in a global, industry-leading CRO.
- Inclusive Culture: We are dedicated to fostering a diverse and accessible workplace where everyone belongs.
Ready to Advance Your Career?
If you have a passion for clinical research and meet the requirements, we would love to hear from you.
