safety specialist - Oakville - beBeePharmacovigilance

    beBeePharmacovigilance
    beBeePharmacovigilance Oakville

    2 weeks ago

    Job title: Pharmacovigilance Associate

    Description

    Job Opportunity

    We are seeking a skilled professional to join our Pharmacovigilance team.

    Key Responsibilities:

    • Recognize and process Adverse Event (AE) / Adverse Drug Reactions (ADR) / Adverse Drug Experience (ADE), Medical Device Incident (MDI) information from source documents.
    Achieve excellent communication skills with internal and external stakeholders by delivering clear concise updates on AE/ ADR/ADE/MDI reports. Identify opportunities for reconciliation of discrepancies in submission to external bodies such as Health Canada or the US-FDA.
    Ensure compliance with GDP standards through precise documentation practices at all times during data analysis.

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