Pharmacovigilance safety Associate openings – Bangalore

Pharmacovigilance safety Associate openings - Bangalore
    • Full Time
    • Bangalore
    • ₹350000 - 500000 INR / Month

    Navitas Lifesciences Hiring Notification for Pharmacovigilance SAFETY ASSOCIATE – I/II

    Job Description

    We are currently seeking a Safety Associate I/II to support our work with Aggregate Reporting, Signal Management, and Risk Management Plans. Within the role you will:

    Location : Bangalore, India

    Education : Graduate or Post-Graduate degree in Life Sciences, Pharmacy, Medicine, Dentistry, Allied Health Sciences, and any other additional related courses

    Role : Associate

    Vacancies – Pharmacovigilance and Safety

    Aggregate Reporting

    • Conduct the authoring and review of Aggregate Safety Reports (i.e. DSURs, PBRERs, PSURs, PADERs, and Canadian Aggregate Reports) and any other aggregate reports as per the requirement of the project
    • Review Aggregate Safety Data from the database and generate Line Listings (LL) and Summary Tabulations (ST) and include the LL and ST in the appropriate template.
    • Analyze safety and regulatory data provided by the client and prepare complete Aggregate Reports according to the client’s requirements.
    • Perform literature screening for inclusion of significant safety articles in the respective section of aggregate reports
    • Compile benefit-risk evaluation sections provided by medical reviewers, as applicable.
    • Ensure compliance with internal and external timelines
    • Address comments from internal and external/client reviewer
    • Finalize reports as per client requirements
    • Participate in internal and external audits and inspections by clients and health authorities

    Signal Management and Risk Management Plans

    • Conduct screening, data mining, and frequency tabulation for potential signals including signal estimation using appropriate signal detection tool as per the client requirement.
    • Generate line listings and summary tabulations from Argus/client safety database.
    • Draft Signal detection, validation, assessment, and benefit-risk analysis and prioritization of signals by reviewing available data.
    • Ensure compliance to appropriate signal SOPs, conventions, and guidelines for all activities performed.
    • Track identified signals from the regulatory and internal signal detection process and monitor the status of signals: potential signals, open signals, refuted signals, and validated signals.

    Desirable Skills and Experience

    • Sound knowledge of the PV domain and working experience in Aggregate Reporting, Signal Management, and Risk Management Plans
    • Good knowledge of DSURs, PBRERs, PSURs, PADERs, and Canadian Aggregate Reports
    • Excellent computer skills and knowledge of MS Office including Word, Excel, and PowerPoint
    • Excellent organizational and time management skills

    Apply Now

     

    To apply for this job please visit www.navitaslifesciences.com.

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