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    Pharm D Job at ProPharma | Apply for Pharmacovigilance Specialist Job Role

    Pharm D Job at ProPharma | Apply for Pharmacovigilance Specialist Job Role

    ProPharma, a trusted global partner in regulatory sciences, clinical research, and pharmacovigilance, is hiring for the Pharmacovigilance Specialist role in India. This Pharm D job opportunity is a full-time pharma job ideal for professionals passionate about drug safety and regulatory excellence. The role focuses on case processing, safety assessment, and ensuring compliance with global pharmacovigilance standards.

    Job Details: Pharm D Job Opportunity

    • Job Position: Pharmacovigilance Specialist
    • Location: India
    • Job Type: Full-Time
    • Job Requisition ID:  8350

    About the Company

    For over 20 years, ProPharma has advanced global health by supporting biotech, med-tech, and pharmaceutical organizations through a full product lifecycle. With expertise in regulatory sciences, clinical research, quality & compliance, pharmacovigilance, and R&D technology, ProPharma delivers customized consulting solutions that accelerate drug and device development.

    Job Description

    The Pharmacovigilance (PV) Specialist is responsible for managing individual case safety reports (ICSRs) and ensuring adherence to regulatory standards. The specialist performs case-level assessments, prepares medical narratives, and supports reporting to global health authorities. This role contributes to patient safety, compliance, and operational excellence across all pharmacovigilance functions, making it an ideal Pharm D job.

    Key Responsibilities

    • Process daily adverse event cases (clinical trial and post-marketed).
    • Perform coding using MedDRA and determine seriousness and expectedness.
    • Conduct follow-ups and identify additional information needed for cases.
    • Create, review, and finalize case narratives for submission.
    • Notify clients as per case management protocols.
    • Support the development and delivery of pharmacovigilance training materials.
    • Highlight discrepancies or quality concerns to senior PV staff or management.
    • Stay updated on global safety regulations and reporting standards.
    • Perform peer reviews for accuracy, consistency, and compliance.
    • Execute additional tasks as assigned by the team lead or manager.

    Educational Qualification

    Pharm D Graduates

    Experience and Skills

    • Minimum 2 years of relevant experience in pharmacovigilance or drug safety, a crucial factor for securing a Pharm D Job.
    • Strong verbal and written communication skills.
    • Excellent attention to detail and accuracy.
    • Ability to analyze and resolve problems effectively.
    • Capable of working independently and collaboratively.
    • Strong organizational and time management skills.
    • Sound understanding of pharmacovigilance principles.

    APPLY ONLINE HERE

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