Drug Safety Associate - Bilingual - French
Core
Receive, document, and triage adverse event information and product quality complaints for Cencora's patient and provider support and pharma commercialization services in Canada.
Role type
Drug Safety Associate (Pharmacovigilance)
Builds
Adverse event reports and product quality complaint databases for Canadian pharma clients
Domain
Healthcare / Pharmacovigilance
Deliverable
client delivery
Required skills
Data entry, source data verification, medical literature screening, report reconciliation, transcription/translation/redaction, solicited follow-up letter preparation, non-conformance/CAPA process support
Preferred skills
Life Sciences degree, Medical Information/Clinical Research experience, Medical terminology knowledge, Health Canada/FDA/EMEA/ICH guidelines knowledge
Technologies
Microsoft Office (Word, Excel, PowerPoint), Program specific databases
Responsibilities
Receive, scan, and document clinical information; Review source data documents and triage adverse events; Perform quality checks on adverse event reports; Assist with source data verification; Screen medical literature for safety info; Prepare reconciliation reports; Conduct solicited follow-ups; Participate in CAPA process
Seniority
Junior to Mid-level, hands-on IC
