Job Summary

• ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
• The role involves assisting in regulatory document preparation, coordinating approvals, maintaining records, and supporting study team documentation.
• ICON offers a competitive salary, diverse benefits focused on well-being and work-life balance, and a commitment to an inclusive and accessible environment.

Matching Summary

Skills & Requirements

Key Requirements

• Bachelor's degree in life sciences
• Previous clinical research experience preferred
• Previous regulatory affairs experience preferred
• Strong attention to detail
• Organizational skills
• Excellent communication skills
• Interpersonal skills
• Ability to work independently
• Manage multiple tasks simultaneously

Work Rights