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    Pharmacovigilance Services Associate

    Accenture
    0-2 years
    Not Disclosed
    Chennai
    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 Associate

    Skill Required: Pharmacovigilance & Drug Safety Surveillance
    Location: [Insert Location]
    Experience: 0-3 Years
    Qualification: Bachelor of Pharmacy/Bachelor of Physiotherapy/BSc. Nursing

    About Accenture

    Accenture is a global professional services company with deep expertise in digital, cloud, and security solutions. We combine unmatched industry experience and specialized skills across over 40 industries, delivering Strategy and Consulting, Technology and Operations services, and Accenture Song services. We are powered by the world’s largest network of Advanced Technology and Intelligent Operations centers, employing over 699,000 people serving clients in 120+ countries. At Accenture, we leverage technology and human ingenuity to drive meaningful change for our clients, partners, and communities. Learn more at www.accenture.com.

    Job Overview

    As a Pharmacovigilance Services Associate, you will be part of the Life Sciences R&D vertical, contributing to pharmacovigilance and drug safety efforts. This role involves creating and managing Individual Case Safety Reports (ICSRs), including data entry, MedDRA coding, case processing, and follow-ups for both Serious and Non-serious cases. You will ensure that all processes comply with global regulatory requirements and client guidelines while supporting the overall safety and regulatory efforts of biopharma clients.

    Roles and Responsibilities

    • Case Management: Handle case identification, data entry, MedDRA coding, case processing, and submission of ICSRs in the safety database.
    • Follow-Up: Perform follow-up tasks for Serious and Non-serious cases in alignment with client guidelines.
    • Problem Solving: Address routine challenges based on general guidelines and precedents.
    • Collaboration: Interact primarily within your own team and with your direct supervisor.
    • Learning & Development: Adapt to new assignments, with detailed instructions and moderate guidance on daily tasks.
    • Shift Work: The role may involve working in rotational shifts.

    Skills and Qualifications

    • Bachelor’s degree in Pharmacy, Physiotherapy, or Nursing (BSc).
    • 0-3 years of experience in Pharmacovigilance, Drug Safety, or a related field.
    • Strong team collaboration skills and the ability to perform well under pressure.
    • Adaptability and the ability to quickly learn new processes.
    • Proficiency in English (verbal and written communication).

    What We Are Looking For

    • Agility: Ability to quickly adapt to new tasks and responsibilities.
    • Team Player: Ability to work effectively within a team structure.
    • Problem-Solving: Capable of resolving routine issues with guidance.
    • Pressure Handling: Able to perform efficiently under pressure and meet deadlines.

    Why Accenture?

    • Career Growth: Opportunity to gain hands-on experience in pharmacovigilance within the Life Sciences sector.
    • Global Exposure: Work with industry leaders in biopharma to help shape the future of healthcare.
    • Learning Environment: Continuous learning and development through structured training programs.

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