ICON plc is a global leader in healthcare intelligence and clinical research, dedicated to advancing medical science through innovative clinical trials. With a commitment to excellence and inclusivity, ICON fosters a dynamic work environment that drives innovation in clinical development.
Job Description
As a Clinical Trial Administrator (CTA) at ICON plc, you will play a crucial role in supporting clinical trials, ensuring compliance with protocols, and contributing to groundbreaking medical research.
Key Responsibilities:
✔ Assist in coordinating and administering clinical trials, ensuring adherence to regulatory standards.
✔ Maintain and organize essential trial documentation, including study files and regulatory submissions.
✔ Support the preparation of study materials such as informed consent forms and case report forms.
✔ Collaborate with cross-functional teams to facilitate smooth trial execution.
✔ Track and report clinical trial progress, milestones, and key metrics.
Qualifications & Skills:
✅ Bachelor’s degree in a scientific or healthcare-related field.
✅ Prior experience or strong interest in clinical research.
✅ Knowledge of clinical trial processes, regulations (ICH-GCP), and guidelines.
✅ Excellent organizational, communication, and teamwork skills.
✅ Ability to work efficiently in a fast-paced environment with attention to detail.
Why Join ICON plc?
ICON offers a competitive salary and a comprehensive benefits package, including:
- Generous annual leave
- Health insurance for you and your family
- Retirement planning options
- Global Employee Assistance Programme (LifeWorks) – 24/7 professional support
- Life assurance
- Flexible benefits (childcare vouchers, gym discounts, travel passes, and more)
ICON is an equal opportunity employer, committed to fostering an inclusive workplace free from discrimination.
