CDC II

As a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Requirements

• Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
• Understanding of clinical trial documents (protocols, case report forms, data management plans, study reports) and processes
• Preferred 2-5 years relevant work experience, or equivalent combination of training and experience.
• Experience with electronic data collection systems.
• Experience managing multiple work deliverables and deadlines.
• Knowledge of data management best practices & technologies as applied to clinical trials.
• Knowledge of FDA and ICH regulations and industry standards applicable to data capture and data management process.
• Strong attention to detail, and organizational skills
• Good time management skills
• Quick learner and comfortable learning new technologies and systems
• Advanced knowledge of office software (Microsoft Office).
• Demonstrated good communication and project management skills

Benefits

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