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Clinical Trials Jobs in ICON plc Careers

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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.

How to Apply

Application Link

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