Operations Specialist 1

IQVIA

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.
  • Liaise with different functional team members and healthcare professionals to address project-related issues.

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
  • Write narratives
  • Liaise with functional teams
  • Bilingual English fluency

Nice-to-have

  • French fluency is a plus
  • Clinical research services
  • Commercial insights
  • Healthcare intelligence

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter