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    Accenture Hiring Pharmacovigilance Services Associate | PV Drug Safety Job in Chennai

    Pharmacovigilance Job at Accenture| PV Services Associate Role for B Pharm & M Pharm 

    Accenture global professional services company Accenture is offering a pharmacovigilance job in Chennai for freshers and early professionals looking to build a strong career in Drug Safety and Life Sciences R&D. This job is ideal for B Pharm and M Pharm graduates Interested in global PV operations.

    • Job Title: Pharmacovigilance Services Associate
    • Job Number: AIOC-S01650757
    • Job Location: Chennai, Tamil Nadu, India

    About the Company

    Accenture is a global professional services company operating in over 120 countries, delivering solutions in strategy, consulting, technology, and operations. In this pharmacovigilance job, Accenture’s Life Sciences R&D team supports global pharma clients with drug safety, regulatory services, and clinical operations.

    This job focuses on ensuring patient safety through ICSR case processing, safety database management, and compliance with global pharmacovigilance standards.

    Job Description

    In this pharmacovigilance job at Accenture, you will be part of the Life Sciences R&D – Drug Safety team responsible for ensuring accurate and compliant handling of global safety data. This pharmacovigilance job involves end-to-end ICSR case processing, including case intake, data entry, MedDRA coding, and maintenance of safety databases as per regulatory guidelines.

    You will also support timely adverse event reporting, case follow-ups, and quality checks to ensure data integrity across the pharmacovigilance lifecycle. This job plays a key role in maintaining patient safety and regulatory compliance for global pharmaceutical clients.

    Key Responsibilities

    • Handle ICSR intake and case processing in this pharmacovigilance job
    • Perform accurate data entry and MedDRA coding
    • Support case follow-ups and safety tracking
    • Ensure regulatory compliance in all pharmacovigilance job tasks
    • Maintain audit-ready documentation and reporting
    • Support global safety submissions
    • Conduct case validation and quality checks
    • Ensure accuracy and consistency in safety databases
    • Improve overall data integrity in this pharmacovigilance job
    • Work within a structured PV operations team
    • Follow SOPs and regulatory guidelines
    • Coordinate with supervisors for task updates and escalations

    Eligibility Criteria 

    • Education: Bachelor’s Degree in Pharmacy; Postgraduate Degree in Pharmacy preferred
    • Experience: Prior experience preferred in Medical Affairs, Medical Writing, Clinical Research, Scientific Research, Consumer Health, or Pharmaceutical Industry
    • Candidates with relevant exposure to pharmacovigilance or drug safety operations will be an added advantage

    Required Skills

    • Knowledge of pharmacovigilance job & drug safety basics
    • Understanding of ICSR case processing & MedDRA coding
    • Strong attention to detail & data accuracy
    • Good documentation & reporting skills
    • Familiarity with regulatory compliance guidelines
    • Analytical thinking & problem-solving ability
    • Ability to work in structured, SOP-driven environments

    Why Join Accenture?

    This pharmacovigilance job at Accenture offers a strong entry into global drug safety operations within a structured Life Sciences R&D environment. You get hands-on exposure to ICSR case processing, MedDRA coding, and regulatory compliance workflows that build a solid foundation in pharmacovigilance.

    This job also provides the opportunity to work with global pharma clients, follow international safety standards, and develop expertise in end-to-end PV operations—making it ideal for long-term career growth in Drug Safety, Clinical Research, and Regulatory Affairs.

    CLICK HERE TO APPLY ONLINE

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