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    Pharmacovigilance Services Associate

    Accenture
    1-3 years
    Not Disclosed
    Bangalore
    10 Oct. 9, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job Description

    Position: Pharmacovigilance Services Associate
    Skills Required: Pharmacovigilance & Drug Safety Surveillance
    Qualifications: Bachelor of Pharmacy
    Experience: 1 to 3 years
    Language Proficiency: Advanced English

    About Accenture

    Accenture is a global professional services company renowned for its capabilities in digital, cloud, and security solutions. With expertise across more than 40 industries, we provide comprehensive services in Strategy and Consulting, Technology and Operations, and Accenture Song—powered by the world's largest network of Advanced Technology and Intelligent Operations centers. Our team of 699,000 professionals is dedicated to delivering technology and human ingenuity to clients in over 120 countries, driving change to create value and shared success for clients, employees, shareholders, partners, and communities. Visit us at www.accenture.com.

    Role Overview

    As a Pharmacovigilance Services Associate aligned with our Life Sciences R&D vertical, you will support biopharma companies in enhancing patient outcomes through clinical trials, regulatory services, and pharmacovigilance. Your responsibilities will include managing the Affiliate Mailbox, reconciling reports, and conducting follow-ups on both Serious and Non-serious cases.

    Key Responsibilities

    • Handle case identification, data entry, MedDRA coding, and case processing in the safety database according to client guidelines and global regulatory requirements.
    • Manage routine problem-solving by referring to established precedents and general guidelines.
    • Interact primarily with your team and direct supervisor, following detailed instructions for daily tasks and new assignments.
    • Contribute as an individual within a team, focusing on a specific scope of work.
    • Be prepared to work in rotational shifts as required.

    What We Are Looking For

    • Ability to solve routine issues with a focus on precedent and general guidelines.
    • Expected interactions within your team and direct supervision.
    • A moderate level of instruction provided for daily tasks and new assignments.
    • Decision-making impacts your own work.
    • Team-oriented with a predetermined scope of work.

    Join us in advancing healthcare through effective pharmacovigilance!

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