Apply pharmacovigilance expertise remotely with Cencora as a Drug Safety Associate supporting Innomar Strategies in Canada. Review safety data, complaints, and clinical information.

This full time, six-month contract supports patient and provider services and pharmaceutical commercialization. The role requires adverse event triage, database entry, source data review, and quality checks. You will work with internal and external clients to clarify information and complete documentation.

Key Responsibilities:
Receive, scan, and document pertinent clinical information
Review source documents and triage adverse event information
Enter adverse events and quality complaints into databases
Perform quality checks and source data verification
Screen medical literature for safety information

Requirements:
Minimum college-level education required
One to three years’ related experience
Knowledge of pharmacovigilance guidelines and industry practices
Robust analytical, organizational, and communication skills
Microsoft Office skills and reliable internet for work from home

Use analytical, detail-focused pharmacovigilance skills to support Cencora’s remote Drug Safety Associate contract.

📌 Remote Drug Safety Associate Toronto (Canada)
🏢 World Courier
📍 Canada