Not specified; competitive within country; benefit...
Fully remote
Regulatory document preparation and submission
Electronic document management systems etmf ectd
Minimum 3 years regulatory publishing experience
ICON is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development
Job Summary
ICON is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development.
The role involves overseeing the preparation, compilation, and submission of regulatory documents for clinical trials using eTMF and eCTD systems.
Candidates will benefit from competitive salary, health insurance, retirement planning, and a global Employee Assistance Programme focused on well-being.
Matching Summary
ICON is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development.
Salary
Not specified; Competitive within country; Benefits include annual leave, health insurance, retirement planning, and flexible options
Skills & Requirements
Must-have
Regulatory document preparation and submission
Electronic document management systems eTMF eCTD
Minimum 3 years regulatory publishing experience
Bachelor's degree in scientific field
Nice-to-have
Canadian submission background preferred
Advanced degree in related field
Process optimization and efficiency skills
Cross-functional collaboration abilities
Key Requirements
3+ years regulatory publishing experience in pharma biotech or CRO