Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2)

The Pharmacovigilance Scientist 2 is responsible for signal detection and literature lead, or back-up lead, to contribute to the conduct of ongoing literature safety surveillance for marketed and investigational products. The role also involves authoring and finalizing aggregate reports, as well as responding to regulatory agency inquiries.

Requirements

• Life science graduate/post-graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
• 4-6 years of relevant experience in Pharmacovigilance including hands-on experience of drug safety, aggregate reports, signal detection/signal management preferred
• Excellent communication (written and verbal) skills
• Team working
• English – fluent (spoken, written)