Instagram
youtube
Facebook

Pharmacovigilance Services Associate

1-3 years
Not Disclosed
10 Nov. 14, 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 Description – Pharmacovigilance Services Associate

Skill Required:

Pharmacovigilance Services – Pharmacovigilance & Drug Safety Surveillance

Designation:

Pharmacovigilance Services Associate

Qualification:

Bachelor of Pharmacy (B.Pharm)

Experience Level:

1 to 3 years


About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With deep expertise across 40+ industries, we offer:

  • Strategy & Consulting

  • Technology

  • Operations

  • Accenture Song

These services are powered by the world’s largest network of Advanced Technology and Intelligent Operations Centers.

With 699,000 employees serving clients in 120+ countries, Accenture delivers innovation and human ingenuity to help organizations create value and drive meaningful change.


Role Overview

You will work within the Life Sciences R&D vertical, supporting global biopharma clients across:

  • Clinical trial operations

  • Regulatory services

  • Pharmacovigilance

  • Patient services

You will be part of the Clinical, Pharmacovigilance & Regulatory sub-offering, contributing to improved patient outcomes by combining scientific expertise with deep insights into patient safety.


Key Responsibilities

1. Safety Case Processing

  • Manage case identification, data entry, MedDRA coding, and case processing for ICSRs (Serious & Non-serious).

  • Perform follow-up activities according to client guidelines.

  • Ensure accurate case submission in safety databases as per global regulatory requirements.

2. Affiliate Mailbox & Report Management

  • Monitor and manage the Affiliate Safety Mailbox.

  • Perform reconciliation of safety reports as per defined processes.

  • Execute written follow-up attempts for both serious and non-serious cases.

3. Compliance & Documentation

  • Maintain compliance with:

    • Client SOPs

    • Global regulatory requirements

    • Pharmacovigilance guidelines

  • Support documentation accuracy and quality during case handling.


What We Are Looking For

  • Knowledge or interest in Cosmetovigilance (Cosmetic product safety surveillance).

  • Strong understanding of pharmacovigilance principles and regulatory expectations.


Roles & Responsibilities (Workstyle Expectations)

  • Solve routine problems using established guidelines and standard procedures.

  • Work under detailed to moderate instruction for daily tasks; receive detailed guidance for new assignments.

  • Interact primarily with your team members and direct supervisor.

  • Work as an individual contributor with a focused scope.

  • May work in rotational shifts, based on business needs.