Senior Small Molecule Regulatory Consultant

Lead small molecule regulatory consulting for Syneos Health across EMEA, the United States, and Canada, using regulatory assessment and communication expertise. Support product maintenance, reporting, and surveillance activities.This senior consultant role requires knowledge of North America’s regulatory affairs framework and drug development concepts. You will assess regulatory guidelines, understand requirements for maintaining marketed products, and contribute systematically to related projects. Strong written and verbal communication supports effective collaboration within team environments and customer-focused solutions.Key Responsibilities:
Apply North America regulatory affairs framework knowledgeAssess and understand applicable regulatory guidelinesUnderstand product maintenance, reporting, and surveillance processesPlan and prioritize work systematically and efficientlyContribute effectively within team environmentsRequirements:
Bachelor’s, Master’s, or PhD degreePreference for life-science or regulatory affairs educationTypically eight years’ pharmaceutical or biotech experienceUnderstanding of drug development conceptsStrong written and verbal communication skillsBring senior regulatory consulting experience, small molecule knowledge, and structured communication to Syneos Health’s global customer work.
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