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    Pharmacovigilance Services Associate

    Accenture
    1-3 years
    Not Disclosed
    Bangalore
    10 Aug. 21, 2024
    Job Description
    Job Type: Full Time Education: B.Pharm/ M.Pharm/ B.Sc/ M.Sc/ Any Life Science Graduate 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: Pharmacovigilance Services Associate

    Skill Required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance
    Designation: Pharmacovigilance Services Associate
    Qualifications: Master of Pharmacy
    Years of Experience: 1 to 3 years

    About Accenture

    Accenture is a global leader in professional services, with extensive expertise in digital, cloud, and security solutions. Leveraging unmatched experience and specialized skills across over 40 industries, we offer 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 699,000 professionals deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Embracing the power of change, we create value and shared success for our clients, people, shareholders, partners, and communities. Learn more at www.accenture.com.

    Role Overview

    As a Pharmacovigilance Services Associate at Accenture, you will be part of our Life Sciences R&D vertical, contributing to pharmacovigilance and drug safety surveillance. This role involves managing the Affiliate Mailbox, reconciling reports, and handling follow-ups for both serious and non-serious cases. You will be responsible for case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for Individual Case Safety Reports (ICSRs) in the safety database, adhering to client guidelines and global regulatory requirements.

    Key Responsibilities

    • Case Management: Identify, enter data, code with MedDRA, process, and submit Individual Case Safety Reports (ICSRs) in the safety database.
    • Report Reconciliation: Reconcile reports per process guidelines and perform follow-ups for both serious and non-serious cases.
    • Compliance: Ensure all activities comply with client guidelines and applicable global regulatory requirements.
    • Documentation: Maintain accurate records and perform follow-ups as needed.

    What We’re Looking For

    • Problem-Solving: Ability to address routine problems using established guidelines and precedents.
    • Team Interaction: Interact primarily with your own team and direct supervisor.
    • Instruction and Guidance: Receive detailed to moderate instructions for daily tasks and comprehensive instructions for new assignments.
    • Impact: Decisions will primarily impact your own work and contribute to team objectives.
    • Shift Work: Willingness to work in rotational shifts as required.

    Join Us

    At Accenture, we are dedicated to fostering a diverse and inclusive work environment. If you have a Master of Pharmacy and 1 to 3 years of experience in pharmacovigilance operations, apply now to be part of our innovative team and make a significant impact in the world of life sciences.

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