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Gn Industry Ls Pharmacovigilance Analyst

2-5 years years
Not Disclosed
10 Aug. 26, 2025
Job Description
Job Type: Full Time Education: MBA from a Tier 1 institute OR equivalent relevant industry experience 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 Title: GN Industry LS Pharmacovigilance Analyst

Designation: Management Consulting Analyst
Job No: R00281976
Employment Type: Full-time
Experience Required: 2–5 years
Location: Bengaluru (Other locations: Gurgaon, Hyderabad, Mumbai also applicable)
Management Levels: 09, 11


About the Role

As a Research & Development Consultant – Life Sciences, you will join Accenture’s Management Consulting team supporting clients in the Life Sciences (LS) industry, with a focus on Pharmacovigilance (PV), R&D, and Regulatory Reporting. You’ll bring a consulting mindset and business acumen to help pharmaceutical and biotechnology companies improve their clinical and regulatory operations through digital and strategic transformation.


Key Responsibilities

  • Support Life Sciences R&D and Pharmacovigilance consulting projects

  • Provide business and operational insights to clients across:

    • Clinical development and clinical operations

    • Pharmacovigilance and safety reporting

    • Regulatory affairs and quality management systems

  • Utilize core consulting tools and techniques including:

    • Issue trees

    • Operating models

    • Business process mapping

    • Implementation frameworks

    • Diagnostic tools (e.g., client questionnaires and structured analyses)

  • Collaborate on transformation initiatives involving:

    • Decentralized clinical trials

    • Lab and quality systems

    • Regulatory information management


Required Qualifications

  • Education:

    • MBA from a Tier 1 institute OR equivalent relevant industry experience

  • Experience:

    • 6+ years of business and/or consulting experience

    • Minimum 1 year of experience in the Life Sciences industry

    • Hands-on management consulting or business consulting experience is mandatory


Desired Skills

  • Strong understanding of Life Sciences R&D, especially:

    • Laboratory functions (R&D and QC labs)

    • Clinical trials (traditional and decentralized)

    • Pharmacovigilance and safety databases

    • Regulatory and quality systems

  • Familiarity with digital tools and platforms such as:

    • Medidata / RAVE (clinical data platforms)

    • Veeva Clinical Suite / RIM (regulatory and clinical systems)

    • ArisG, ARGUS (pharmacovigilance databases)

    • Lab Informatics tools

  • Strong analytical and communication skills

  • Ability to work across teams and clients in a consulting capacity


About Accenture

Accenture is a global professional services company with expertise in digital, cloud, and security. With over 699,000 employees serving clients in 120+ countries, Accenture delivers services in:

  • Strategy & Consulting

  • Technology

  • Operations

  • Accenture Song

We combine human ingenuity and cutting-edge technology to help the world’s leading businesses solve their toughest challenges and deliver sustainable growth.
Visit us: www.accenture.com


Important Notes

  • This role is part of Accenture's Life Sciences Management Consulting practice

  • Travel may be required based on project needs and client location

  • The role may involve working with cross-functional global teams


Save, Share, or Apply Now via the Accenture Careers Portal.