Safety PV Professional

2 weeks ago

Bengaluru Bangalore Pune Chennai, India beBeePharmacovigilance Full time US$ 9,00,000 - US$ 12,00,000
">Pharmacovigilance Specialist

We are seeking a highly skilled Pharmacovigilance Specialist to join our team. This role is responsible for the collection, processing, and reporting of adverse event data, ensuring compliance with global regulations and company standards.

Responsibilities:
  • Case Processing:
    • Manage Individual Case Safety Reports (ICSRs) including data entry, coding of adverse events using MedDRA, and drug coding using WHO-DD.
    • Timely and accurate processing of adverse event reports from various sources (e.g., clinical trials, spontaneous reports, literature).
    • Comprehensive review of case information to ensure data quality and integrity.
  • Regulatory Reporting:
    • Prepare and submit expedited and periodic safety reports to global health authorities within required timelines.
    • Ensure all reporting activities are in full compliance with ICH guidelines, GVP modules, and other relevant local and international regulations.
    • Assist in the preparation of aggregate reports such as PSURs/PBRERs.
  • Quality & Compliance:
    • Participate in internal and external audits and inspections, ensuring readiness and addressing any findings.
    • Maintain and update pharmacovigilance documentation, including SOPs and safety management plans.
    • Quality control checks on processed cases to ensure accuracy and consistency.
Requirements:
  • A degree in a life sciences, medical, or pharmacy-related field.
  • Proven experience in a pharmacovigilance or drug safety role.
  • Strong understanding of pharmacovigilance principles, processes, and global regulations.
  • Proficiency with safety databases such as ARGUS, ARISg, or a similar system.
  • Knowledge of MedDRA and WHO-DD coding.
  • Excellent attention to detail, strong analytical skills, and a commitment to data accuracy.
  • Effective communication and interpersonal skills.

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