ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
The role involves preparing, compiling, and submitting regulatory documents such as CT/IND, MAA/NA, variations, DSUR, PSUR, and renewals while collaborating with cross-functional teams.
ICON offers competitive salaries and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
Skills & Requirements
Must-have
Regulatory submission processes
Clinical trial document preparation
Label review and translation management
Regulatory intelligence participation
Cross-functional team collaboration
Nice-to-have
Strong attention to detail
Excellent communication skills
Business development facilitation
Inclusive and diverse work culture
Key Requirements
Bachelor's degree in scientific or healthcare field
2-3 years regulatory affairs experience
Proficiency in CT/IND and MAA/NA submissions
Familiarity with DSUR, PSUR, and renewals
Experience in pharmaceutical or biotechnology industry