PV Physician-KunTuo
Core
Review, assess, and process safety data and adverse events (AE) information across service lines, distributing reports to internal and external third parties per regulations.
Role type
Junior Pharmacovigilance Safety Associate
Builds
Safety databases, case narratives, and regulatory reports for life sciences clients
Domain
Life Sciences / Pharmacovigilance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Medical terminology, Safety database navigation, Global/regional clinical research regulatory knowledge, Attention to detail, Microsoft Office proficiency, Time management, Problem solving, Team collaboration
Preferred skills
None stated
Technologies
Safety databases, Microsoft Office, Web-based applications
Responsibilities
Prioritize and complete assigned trainings, Process safety data per SOPs, Perform pharmacovigilance activities including collecting/tracking AE information, Determine initial/update status of incoming events, Perform database entry, Code AE and products, Write narratives, Create and track cases, Identify quality problems, Mentor new team members, Attend project team meetings
Seniority
Junior, 1-1.5 years experience
