Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2)

The Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2) will act as 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 will involve authoring and finalizing aggregate reports, responding to regulatory agency inquiries, and serving as a principal owner for the molecule.

Requirements

• Life science graduate/post-graduate, pharmacy, nursing, or 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
• Excellent communication (written and verbal) skills
• Team working
• Fluent English (spoken, written)