Drug Safety Associate - 6-Month Contract
Core
Receive, scan, document, and triage clinical information and adverse event data 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
Domain
Healthcare / Pharmaceutical / Pharmacovigilance
Required skills
Data entry, source data verification, medical terminology, regulatory guideline knowledge (Health Canada, US FDA, EMEA, ICH), analytical skills, attention to detail, computer skills (Microsoft Office)
Preferred skills
Life Sciences degree, bilingual English/French, medical/pharmaceutical field experience
Responsibilities
Receive, scan and document clinical information; Review source data documents and triage adverse event information; Data entry and submission of adverse event information and product quality complaints; Perform quality check on adverse event reports; Assist with source data verification checks; Screen medical and scientific literature for safety information; Prepare reconciliation reports and conduct data clarifications; Assist with non-conformance/CAPA process
Seniority
Junior to Mid-level, 1-3 years experience
