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Pharmacovigilance Services Associate

Accenture
Accenture
1-3 years
Not Disclosed
10 Sept. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Pharmacovigilance Services Associate

Company: Accenture
Location: Bengaluru, India
Job Type: Full-time
Experience Required: 1–3 years
Qualification:

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)
    Skill Area: Pharmacovigilance Operations – Pharmacovigilance & Drug Safety Surveillance


About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With over 699,000 employees across 120+ countries, Accenture combines unmatched experience and specialized skills across more than 40 industries.

Services include:

  • Strategy & Consulting

  • Technology & Operations

  • Accenture Song

Accenture helps clients deliver value by combining scientific expertise with insights into the patient experience, driving innovation and improving healthcare outcomes.

🌐 Visit: www.accenture.com


Role Overview

As a Pharmacovigilance Services Associate, you will be aligned with the Life Sciences R&D vertical and contribute to pharmacovigilance and patient safety services. You will manage the Affiliate Mailbox, reconcile reports, and perform follow-ups for both Serious and Non-serious cases, ensuring compliance with global regulatory requirements and client guidelines.


Key Responsibilities

  • Manage and process reports from the Affiliate Mailbox.

  • Reconcile reports as per defined processes.

  • Perform written follow-ups for both serious and non-serious adverse events.

  • Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database.

  • Solve routine problems using established guidelines and precedents.

  • Interact primarily with your team and direct supervisor.

  • Follow detailed to moderate instructions for daily tasks and new assignments.

  • Work may require rotational shifts.


Candidate Profile

  • Education: B.Pharm / M.Pharm

  • Experience: 1–3 years in pharmacovigilance or related healthcare roles

  • Skills Required:

    • Strong attention to detail

    • Ability to follow structured processes

    • Team collaboration and communication skills


Equal Employment Opportunity

Accenture is an equal opportunity employer. Employment decisions are made without regard to:

  • Age, race, creed, color, religion, sex, national origin, ancestry

  • Disability status, veteran status, sexual orientation, gender identity/expression

  • Genetic information, marital status, citizenship status, or any other protected category


Why Join Accenture?

  • Opportunities for certifications, training, and diverse work experiences

  • Holistic support for physical, mental, and financial health

  • Inclusive and bias-free workplace

  • Recognized as one of the World’s Best Workplaces™


Important Notice

⚠️ No payment is required to apply or secure employment at Accenture.
If contacted for payment, do not respond and report immediately to: india.fc.check@accenture.com


Join Accenture and be at the heart of change.