Apply pharmacovigilance knowledge and analytical skills as a Drug Safety Associate with Cencora. Support adverse event review, documentation, and reporting activities.
This Drug Safety Associate supports clinical information processing within Cencora’s pharmaceutical solutions operations. The position suits candidates with one to three years of Medical Information, Clinical Research, Drug Safety, pharmacy, or pharmaceutical experience. You will communicate with clients, review source documents, enter safety data, and support quality processes. Knowledge of Health Canada, US FDA, EMEA, and ICH pharmacovigilance guidelines is required.
Key Responsibilities: Receive, scan, and document pertinent clinical information
Review source documents and triage adverse event information
Enter adverse events and complaints into databases
Screen medical and scientific literature for safety information
Prepare reconciliation reports and follow-up letters
Requirements: Minimum college-level education required
Life Sciences diploma or degree strongly preferred
One to three years of relevant experience
Robust analytical, organizational, and problem-solving skills
Microsoft Office skills and reliable internet for remote work
Use pharmacovigilance, data entry, and quality review skills to support Cencora’s safety information processes accurately and consistently.