Junior Regulatory Affairs Advisor
Core
Support clients in navigating global regulatory requirements and interpreting EMA, FDA, and National Competent Authority guidance for pharmaceutical and life sciences products.
Role type
Junior Regulatory Affairs Advisor
Builds
Regulatory strategies, submissions, and Health Authority interactions
Domain
Life Sciences / Pharmaceutical Regulatory Affairs
Deliverable
client delivery
Required skills
Regulatory submissions, lifecycle management, regulatory intelligence, Health Authority interactions, RIM platforms, EU pharmaceutical regulation, FDA processes
Preferred skills
Regulatory training/certification (TOPRA, DIA, RAPS), European languages (French, Dutch)
Technologies
Veeva RIM
Responsibilities
Help clients navigate global regulatory requirements; Support clients in interpreting EMA, FDA, and National Competent Authority requirements; Contribute to client regulatory strategies and submissions; Support assessments of Regulatory Affairs processes and systems; Help clients understand the impact of new regulatory requirements; Turn regulatory information into actionable insights
Seniority
Junior, 1-2 years experience
