Senior Clinical Trial Regulatory Advisor

About the role

Syneos Health is looking for a Senior Clinical Trial Regulatory Advisor in Belgrade, working in a hybrid setting. This regulatory delivery professional converts regulatory strategy into accurate, timely and compliant execution, ensuring submission readiness, quality and compliance with applicable requirements.

Key responsibilities

• Prepare, coordinate or oversee clinical-trial submissions
• Work across multiple countries or submission pathways
• Manage submission documentation and dependencies
• Interact with study teams, sites and regulatory stakeholders
• Resolve submission-readiness or quality issues
• Deliver accurate regulatory plans and assumptions, collect and review documents on time, and identify regulatory constraints early

Required profile

• Experience preparing, coordinating or overseeing clinical-trial submissions
• Experience working across multiple countries or submission pathways
• Knowledge of country and regional requirements

Required skills

• Regulatory submission execution
• Planning and document management
• Quality and compliance discipline
• Risk identification
• Cross-functional communication and data and milestone accuracy

The company states that equivalent experience, skills and education will be considered, and that additional tasks may be assigned at its discretion.