Our client’s company with an international scope is seeking a new team member to join its Prague office! Team is smaller but friendly with an international team spirit.

We are looking for a responsible candidate with the knowledge of MedDRA coding for medical review and assesment of Adverse Events.

More specificaly, you will be responsible for:

• Review and verify adverse events
• Provide company comments in accordance with client requirements
• Identify and resolve or escalate case issues and coordinate your work with client therapeutic team
• Ensure follow-up if needed
• Manage source documents and appropriate MedDra codes
• Perform other drug safety related activities as assigned