CDC I

We are seeking a Clinical Data Coordinator I to join our diverse and dynamic team. As a Clinical Data Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Requirements

• Master’s degree in a relevant field (e.g., Life Sciences or Healthcare)
• Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry
• Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar)
• Strong attention to detail and the ability to work effectively in a fast-paced environment
• Excellent communication skills and the ability to collaborate with cross-functional teams

Benefits

• Various annual leave entitlements
• A range of health insurance offerings
• Competitive retirement planning offerings
• Global Employee Assistance Programme
• Life assurance
• Flexible country-specific optional benefits