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Pharmacovigilance Services Associate

1–3 years years
Not Disclosed
10 Sept. 2, 2025
Job Description
Job Type: Full Time Education: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm) 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: Pharmacovigilance Services Associate

Job ID: AIOC-S01564207
Location: Bengaluru, India
Employment Type: Full-Time
Experience Required: 1–3 years


About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. Serving clients in over 120 countries, Accenture combines unmatched experience and specialized skills across more than 40 industries, offering:

  • Strategy & Consulting

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Backed by the world’s largest network of Advanced Technology and Intelligent Operations centers, Accenture employs 699,000+ people worldwide.

🔗 Visit: www.accenture.com


Role Overview

As a Pharmacovigilance Services Associate, you will work within the Life Sciences R&D vertical, supporting the Clinical, Pharmacovigilance & Regulatory teams. You’ll be responsible for case processing, including identification, MedDRA coding, and submission of ICSRs, as well as managing communications and report reconciliations.


Key Responsibilities

  • Manage the Affiliate Mailbox for case intake.

  • Perform reconciliation of reports following standard processes.

  • Execute written follow-ups for both Serious and Non-serious Adverse Events (AEs).

  • Handle case identification, data entry, and MedDRA coding.

  • Conduct ICSR processing, submission, and follow-ups in the safety database.

  • Ensure compliance with client guidelines and global regulatory standards.

  • Work independently within a defined scope; escalate issues as needed.

  • May be required to work in rotational shifts.


Qualifications

  • Education Required:

    • Bachelor of Pharmacy (B.Pharm) or

    • Master of Pharmacy (M.Pharm)

  • Experience:

    • 1–3 years in Pharmacovigilance, Drug Safety, or related fields


Preferred Skills

  • Knowledge of pharmacovigilance operations, case processing, and regulatory requirements

  • Experience with MICC (Medical Information Contact Center) processes

  • Willingness to work in shifts (rotational)

  • Strong written and verbal communication skills

  • Ability to perform under pressure and adapt quickly

  • Detail-oriented and organized


Soft Skills

  • Adaptability & flexibility

  • Problem-solving using precedent/guidelines

  • Collaboration within a team and communication with direct supervisors


Work Environment

You will be part of a team focused on helping global biopharma companies optimize patient outcomes through the integration of scientific expertise and real-world data.


What Accenture Offers

  • Career growth through continuous learning

  • Opportunity to work with global life sciences leaders

  • Exposure to cutting-edge pharmacovigilance systems and processes

  • Inclusion in a diverse, people-centric workplace


How to Apply

🔗 Apply Now on Accenture Careers


Learn More

  • Hiring Process at Accenture

  • Interview Tips

  • Explore Accenture Benefits


Equal Opportunity Statement

Accenture is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or age.