PV Associate

Description

• Processing serious and non-serious adverse events, spontaneously reported adverse reactions and/or other medically related project information such as adverse events of special interest and clinical endpoints.
• Execute literature searches to identify key product articles for signal detection reports, drug safety relevance etc
• Responding to Medical Information (MI) enquiries in a timely fashion and within the timelines as documented in internal procedures

Requirements

• Desirable to have experience having worked in medical information and/or pharmacovigilance preferred
• Must have valid right to work in the United Kingdom
• Excellent communication skills, written and oral and fluent in English
• Qualified up to BSc or equivalent life science degree

Benefits

Training + Development

Interview process

Visa Sponsorship

Security clearance