Support the development, implementation, and execution of regulatory strategies for clinical development programmes
Job Summary
Support the development, implementation, and execution of regulatory strategies for clinical development programmes.
Prepare, review, and coordinate regulatory documents such as clinical trial applications, briefing packages, and responses to health authority questions.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.
Matching Summary
Support the development, implementation, and execution of regulatory strategies for clinical development programmes.
Skills & Requirements
Must-have
regulatory strategy development
regulatory affairs deliverables
global regulatory frameworks
cross-functional team collaboration
health authority interactions
Nice-to-have
foster an inclusive environment
drive innovation and excellence
nurtures talent
well-being and work life balance
Key Requirements
Bachelor's degree in scientific or healthcare field
Experience in regulatory affairs, writing, or clinical development
Good understanding of global regulatory frameworks
Strong scientific, analytical, and critical thinking skills
Excellent written and verbal communication skills
Ability to manage multiple regulatory activities and timelines