Turn detailed safety information into accurate pharmacovigilance records at Cencora. Use solid communication, organization, and problem-solving skills across assigned activities.

As a Drug Safety Associate, you will process adverse event information and product quality complaints for client programs. Cencora seeks candidates with one to three years of experience in Medical Information, Clinical Research, Drug Safety, pharmacy, or pharmaceutical fields. The work includes clarifying information with internal and external clients, conducting quality checks, and supporting source data verification. Current knowledge of Health Canada, US FDA, EMEA, and ICH guidelines is important.

Key Responsibilities:

- Request clarification and additional information from clients




- Perform quality checks on adverse event reports
- Assist with source data verification checks
- Prepare transcription, translation, and redaction activities
- Support non-conformance and CAPA processes

Requirements:

- College-level education is required
- Life Sciences concentration is a strong asset
- Effective oral and written communication skills
- Superior attention to detail and deadline consistency
- Effective interpersonal and multitasking abilities

Bring careful review, client communication, and pharmacovigilance expertise to Cencora’s adverse event and complaint workflows.

📌 Pharmacovigilance Drug Safety Specialist (Canada)
🏢 Innomar Strategies
📍 Canada