Safety Operations Intern-DL 2027
Core
Assist managers in processing adverse drug reaction safety data, including collecting and tracking adverse events (AE) and endpoint information, managing project workflows, database entry, quality control, and preparing safety submission dossiers.
Role type
Safety Operations Intern
Builds
Adverse event databases and safety submission dossiers for life sciences clients
Domain
Life sciences / Pharmacovigilance
Deliverable
client delivery
Required skills
Adverse event data collection, database entry, quality control, report generation, timeline tracking
Preferred skills
Biology or pharmaceutical background
Technologies
None stated
Responsibilities
Collect and track adverse events and endpoint information; Determine initial or updated status of incoming events; Track completion schedules for event handling; Manage project workflows including database entry and quality control; Generate drug safety data reports; Prepare drug safety submission dossiers
Seniority
Intern
