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    Job · 11149997

    ProPharma Group logo

    pharmacovigilance Specialist

    ProPharma Group · Hyderabad · onsite · Posted 71d ago

    Undisclosed3–4 yrsfulltimeSourced fromNaukri

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

    About this role

    Job Summary

    The Pharmacovigilance (PV) Specialist, Case Processing manages individual case safety reports, performs initial case-level assessment of expectedness, confirms seriousness, composes accurate and thorough medical narratives, and generates queries for missing or unclear information. The PV Specialist ensures all cases meeting expedited regulatory reporting criteria are submitted to regulatory authorities in accordance with internal guidelines, Working Practices, SOPs, and applicable safety regulations. The PV Specialist maintains distinctive quality and commitment as the operating philosophy in carrying out all processes, and continually seeks out ways to enhance customer service experience both internally and externally.

    Essential Functions

    • Responsible for daily case processing of adverse event cases (clinical trial and/or post marketed), including coding using MedDRA, determining seriousness and expectedness at the event and case level.
    • Perform case follow up activities such as identification of information to be collected during follow-up.
    • Creating and reviewing case narratives.
    • Providing client notifications as required for case management.
    • Supporting and contributing to the development of training materials and training delivery.
    • Highlight areas of concern/discrepancies to the Principal PV Specialist, Case Processing and/or Manager, Case Processing when related to ICSRs.
    • Acquire and maintain an up-to-date knowledge of global safety regulations for medicines.
    • Peer reviews of cases for quality, consistency, and accuracy as needed.
    • Other duties as assigned

    Necessary Skills and Abilities

    • Strong verbal, written and interpersonal communication skills.
    • High level of accuracy and attention to detail.
    • Ability to identify and resolve problems in a timely manner.
    • Able to work independently and collaboratively in a multi-disciplinary team.
    • Excellent organization and prioritization skills; able to multitask.
    • Basic knowledge of Pharmacovigilance.

    Educational Requirements

    • Required: a Bachelors degree in life sciences.
    • Preferred: advanced degree, RN, RPh, PharmD or equivalent.

    Experience Requirements

    • Two years of related work experience.


    Disclaimer: This job posting & Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

    Sourced from naukri

    Skills

    Customer Servicepharmacovigilanceclinical researchConsultingCase ProcessingcodingPharmaLife SciencesRecruitment

    About ProPharma Group

    ProPharma Group logo

    ProPharma Group

    Clinical Research

    100

    employees

    2001

    25 years old

    Hyderabad / Secunderabad, Telangana

    India

    ₹8.3L PA avg

    Avg at ProPharma Group

    About

    We are #soaringbeyondCRO as the World’s Largest RCO

    Industries

    Clinical Research

    Employee ratings

    10 reviews

    4.2/ 5

    Culture

    4.7

    Career growth

    4.1

    Work-life

    4.9

    Employees rate it well for

    Work-Life Balance43Skill Development43

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