Senior Global Regulatory Scientist

As a Senior Global Regulatory Scientist at ICON, you will support the development, implementation, and execution of regulatory strategies for clinical development programmes. Key responsibilities include regulatory affairs deliverables, regulatory strategy development, preparing and reviewing regulatory documents, and interpreting and applying regulations. The role requires a Bachelor's degree in a relevant scientific discipline or healthcare-related field, experience in regulatory affairs, and strong scientific, analytical, and critical thinking skills.

Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Experience in regulatory affairs, regulatory writing, or clinical development within the pharma, biotech, or CRO industry
• Good understanding of global regulatory frameworks and guidelines relevant to clinical development
• Strong scientific, analytical, and critical thinking skills, with the ability to interpret complex data and regulations
• Excellent written and verbal communication skills, with high attention to detail and accuracy
• Ability to work effectively in cross-functional teams and manage multiple regulatory activities and timelines
• Willingness to travel as required (approximately 5%)

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