Regulatory Affairs Specialist

Work Schedule
Standard Office Hours (40/wk)
Environmental Conditions
Office
Job Description
Join Us as a Regulatory Affairs Specialist for clinical trials – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you’ll have the opportunity to provide innovative solutions, including regulatory expertise and client interface, to offer strategic intelligence and guidance supporting product development from preclinical stages through registration and product optimization. As a Regulatory Affairs Specialist, you'll provide strategic, expedient, and efficient preparation of client deliverables that meet current local, regional, and ICH regulatory and technical requirements. Additionally, you will act as a liaison with internal and external clients in the provision and marketing o...