🛠 Tech Stack

💼 About This Role

You'll provide regulatory development advice and guidance for clinical trials, ensuring timely, compliant submissions. You'll coordinate with project teams and regulatory authorities. This role offers the chance to impact drug development at a leading clinical solutions company.

🎯 What You'll Do

• Compile and coordinate regulatory submissions to authorities
• Provide strategic regulatory guidance throughout clinical development
• Serve as regulatory representative at project team meetings
• Oversee Regulatory Affairs Specialists for submission targets

📋 Requirements

• Bachelor's degree in scientific or healthcare discipline
• 5+ years regulatory affairs experience
• Knowledge of drug development processes and regulatory milestones
• Fluent English