
Regulatory Affairs Consultant - Clinical Regulatory Affairs
Parexel seeks a Regulatory Affairs Consultant to develop and execute regulatory strategies, lead health authority interactions and manage regulatory submissions (INDs, annual reports, safety submissions) for a dedicated pharma client. Requires minimum 5+ years in regulatory affairs, strong knowledge of FDA and ICH guidelines, experience with electronic submission systems (e-STARs), and ability to work independently within cross-functional teams.














