Strong understanding of global regulatory requirements
ICON Clinical Research is seeking a Regulatory Submissions Manager in Kazakhstan to support drug development through regulatory guidance and submissions. The role requires extensive experience in regulatory affairs, particularly with CTA/IND/MAA submissions, and offers a competitive benefits package in an inclusive work environment
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization.
As a Manager, Regulatory Affairs, you will play a pivotal role in drug development.
ICON offers a range of benefits focused on well-being and work-life balance.
Matching Summary
Match Score: 85
ICON Clinical Research is seeking a Regulatory Submissions Manager in Kazakhstan to support drug development through regulatory guidance and submissions. The role requires extensive experience in regulatory affairs, particularly with CTA/IND/MAA submissions, and offers a competitive benefits package in an inclusive work environment.
Skills & Requirements
Must-have
Lead regulatory activities independently
Experience with CTA/IND/MAA submissions
Strong understanding of global regulatory requirements