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    Job · 15682087

    Centric Edu logo

    Pharmacovigilance Associate

    Centric Edu · Hyderabad · onsite · Posted 47d ago

    ₹4.0L - ₹6.5L PA0–3 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    Role & responsibilities

    • Perform Individual Case Safety Report (ICSR) processing, including case intake, data entry, validation, and follow-up.
    • Review and assess adverse event reports from clinical trials, spontaneous sources, literature, and other safety databases.
    • Perform case coding using MedDRA and WHO Drug/appropriate coding dictionaries.
    • Conduct seriousness, expectedness, and causality assessments as per applicable procedures and guidelines.
    • Prepare and submit safety reports within defined regulatory timelines.
    • Perform duplicate checks, quality review, and data reconciliation to ensure accuracy and completeness.
    • Support follow-up activities for missing or incomplete safety information.
    • Maintain accurate documentation and comply with SOPs, GVP guidelines, and regulatory requirements.
    • Assist with aggregate safety reporting, signal detection, and safety data analysis as required.
    • Collaborate with Clinical, Regulatory Affairs, Medical Writing, and other cross-functional teams.
    • Ensure compliance with applicable global pharmacovigilance regulations and company quality standards.

    Preferred candidate profile

    • Bachelors or Masters degree in Pharmacy, Life Sciences, Medicine, Biotechnology, Nursing, or a related field.
    • 03 years of experience in Pharmacovigilance/Drug Safety is preferred; freshers with relevant PV training may also be considered.
    • Good understanding of Pharmacovigilance principles, ICSR processing, adverse event reporting, and safety databases.
    • Knowledge of MedDRA coding and case processing workflows is an advantage.
    • Familiarity with GVP guidelines, ICH guidelines, and regulatory reporting requirements.
    • Experience or training in Argus Safety, Medidata Rave, or other pharmacovigilance databases is preferred.
    • Strong attention to detail and ability to work accurately with safety data.
    • Good written and verbal communication skills.
    • Ability to manage multiple cases and meet strict regulatory timelines.
    • Good analytical, documentation, and problem-solving skills.
    • Willingness to work in a team-oriented and process-driven environment.

    You can share your updated Cv in whatsapp to HR Shruti +[phone removed] or HR Riya +[phone removed]


    Sourced from naukri

    Skills

    Healthcare Domainpharmacovigilanceclinical researchClinicalDrug safetyCase ProcessingPharmacyMedicalPharmaceuticalLife Sciences

    Pharmacovigilance Associate · waiting for your command