(engineering) or related field (or non-US equivalent). A minimum of 5 years' experience in Regulatory Affairs. Advanced... of submissions to the FDA strongly preferred. Regulatory Affairs Certification (US or EU) preferred. A combination of education...
Pharmacovigilance & Drug Safety Specialist (PharmD) Bring your clinical lens to the world of drug safety and reporting.... Key Responsibilities: Analyze adverse event reports and clinical trial safety data. Prepare regulatory submissions (e.g...