Drug Safety Specialist/ Clinical Safety Coordinator

About the role

This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you!

What you'll do

• Determine plan of action for incoming calls; Collect, process, and track incoming adverse and serious adverse events; Write safety narratives

What you need

• Pharmacovigilance
• Clinical research
• Communication
• Any graduate

Good to have

• Pharmacology