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Pharmacovigilance Services Associate

Accenture
Accenture
1-3 years
Not Disclosed
10 Nov. 18, 2025
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

Job Title: Pharmacovigilance Services Associate

Job Category: Pharmacovigilance / Drug Safety

Job Type: Full-Time

Qualification: Bachelor of Pharmacy (B. Pharm)

Experience Required: 1–3 years

Company: Accenture


About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With 699,000+ employees across more than 120 countries, Accenture offers services in Strategy & Consulting, Technology, Operations, and Accenture Song. The company leverages innovation and human ingenuity to create value for clients and communities worldwide.


Role Overview

You will be part of Accenture’s Life Sciences R&D vertical, supporting global biopharma clients across clinical trials, regulatory operations, pharmacovigilance, and patient services.

This position falls under the sub-offering: Clinical, Pharmacovigilance & Regulatory.


Skill Requirement

Pharmacovigilance Services – Pharmacovigilance & Drug Safety Surveillance


Key Responsibilities

Pharmacovigilance Case Processing

  • Manage the Affiliate Safety Mailbox and perform reconciliation of safety reports as per process.

  • Handle ICSR (Individual Case Safety Report) tasks including:

    • Case intake and identification

    • Data entry and quality checks

    • MedDRA coding

    • Case processing and medical evaluation (as applicable)

    • Regulatory submissions

    • Follow-up activities for both serious and non-serious cases

  • Ensure compliance with client guidelines and global regulatory requirements.

Communication & Documentation

  • Perform written follow-up attempts with reporters for missing information.

  • Maintain accurate documentation in the safety database.

Cosmetovigilance (as required)

  • Support cosmetovigilance activities as per project requirements.


General Responsibilities

  • Solve routine problems using established guidelines and procedures.

  • Interact primarily with your internal team and supervisors.

  • Receive detailed instructions for daily tasks and new assignments.

  • Work independently within a defined scope of responsibilities.

  • Role may require rotational shifts.