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 knowledge
• Assess and understand applicable regulatory guidelines
• Understand product maintenance, reporting, and surveillance processes
• Plan and prioritize work systematically and efficiently
• Contribute effectively within team environments

Requirements:

• Bachelor’s, Master’s, or PhD degree
• Preference for life-science or regulatory affairs education
• Typically eight years’ pharmaceutical or biotech experience
• Understanding of drug development concepts
• Strong written and verbal communication skills

Bring senior regulatory consulting experience, small molecule knowledge, and structured communication to Syneos Health’s global customer work.