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    Pharmacovigilance Services New Associate

    Accenture
    0-1 years
    Not Disclosed
    Bangalore
    10 Nov. 7, 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

    Pharmacovigilance Services New Associate

    Skill Required: Pharmacovigilance & Drug Safety Surveillance
    Location: [Insert Location]
    Experience: 0-1 Year
    Qualification: BSc
    Language Proficiency: English - Proficient

    About Accenture

    Accenture is a global leader in professional services, combining digital, cloud, and security expertise to deliver transformative outcomes for clients. Our solutions span across 40+ industries, offering Strategy and Consulting, Technology and Operations, and Accenture Song services, powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. With a workforce of 699,000 employees in 120+ countries, Accenture leverages technology and human ingenuity to drive innovation, growth, and value for our clients and communities. To learn more, visit www.accenture.com.

    Job Overview

    As a Pharmacovigilance Services New Associate, you will work within the Life Sciences R&D vertical, supporting pharmacovigilance services for biopharma clients. Your role will primarily focus on the management and processing of Individual Case Safety Reports (ICSRs) in the safety database. You will perform case identification, data entry, MedDRA coding, and follow-up activities for Serious and Non-serious cases, ensuring compliance with global regulatory requirements and client guidelines.

    Roles and Responsibilities

    • Case Management: Create and manage ICSRs, ensuring accurate data entry, MedDRA coding, and case processing.
    • Data Entry & Coding: Enter case data into the safety database, ensuring compliance with regulatory guidelines.
    • Follow-Up: Perform follow-up activities for both Serious and Non-serious cases as per client requirements.
    • Problem-Solving: Solve routine issues using general guidelines and precedents.
    • Team Collaboration: Work under the supervision of your team lead, collaborating closely with peers.
    • Shift Work: This role may require working in rotational shifts.

    Skills and Qualifications

    • Bachelor's degree (BSc) in a relevant field.
    • 0-1 year of experience in Pharmacovigilance, Drug Safety, or related areas.
    • Knowledge of MedDRA coding and ICSR case processing is desirable.
    • Strong communication skills (written and verbal).
    • Ability to work in a team-oriented environment and handle tasks under supervision.
    • Adaptable and able to perform under pressure.
    • Proficiency in English is required.

    What We Are Looking For

    • Attention to Detail: Ensuring accurate data entry and case processing.
    • Team Player: Ability to work effectively within a team and collaborate with others.
    • Commitment to Quality: Focused on delivering high-quality work in compliance with industry standards.
    • Process-Oriented: Adherence to client guidelines and global regulations.

    Why Accenture?

    • Career Growth: Opportunity to work in a dynamic and innovative environment with a focus on personal and professional development.
    • Global Exposure: Be a part of a globally recognized company with opportunities to work with world-leading biopharma companies.
    • Work-Life Balance: Flexible shift schedules and a collaborative team culture.

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