Senior Associate – Regulatory Affairs (CMC) at ClinChoice

📋 Description

• Oversee new product registrations and post-approval submissions.
• Review and write CMC modules 2 and 3.
• Coordinate regulatory filings for EU and CIS regions.
• Maintain regulatory processes and tracking tools.
• Foster relationships with health authorities and support launches.
• Develop and execute regulatory strategies aligned with the business plan.

🎯 Requirements

• Bachelor’s or Master’s in Life Science/Pharma.
• 4–6 years of relevant experience.
• RAPS certification desirable.