Operations Specialist 1

IQVIA UK

Multiple Locations
Fully remote
Process safety data
Collect and track adverse events
Database entry and coding
Review, assess, and process safety data and information across service lines, received from various sources

Job Summary

  • Review, assess, and process safety data and information across service lines, received from various sources.
  • Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.
  • Ensure compliance with quality, productivity, and delivery standards per project requirements.

Matching Summary

Review, assess, and process safety data and information across service lines, received from various sources.

Skills & Requirements

Must-have

  • Process safety data
  • Collect and track adverse events
  • Database entry and coding
  • Liaise with functional teams
  • 100% remote role

Nice-to-have

  • French fluency is a plus
  • Healthcare professional liaison

Key Requirements

  • Bachelor’s degree in Life sciences
  • C1 level minimum in English
  • Up to 3 years clinical experience
  • 1 year pharmacovigilance experience

Work Rights

Not specified

Tailored Resume

Cover Letter