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Pharmacovigilance Services New Associate

Accenture
Accenture
Freshers years
Not Disclosed
Chennai, India
10 May 11, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Services New Associate – Structured Job Description

Job Overview

Field

Details

Job Title

Pharmacovigilance Services New Associate

Company

Accenture

Job ID

AIOC-S01637902

Location

Chennai

Employment Type

Full-Time

Experience Required

0–1 Year

Qualification Required

Bachelor of Pharmacy (B.Pharm) / B.Sc. Nursing


About the Company

Accenture is a leading global professional services organization specializing in:

  • Digital transformation

  • Technology services

  • Cloud computing

  • Security

  • Operations and consulting

The company operates in more than 120 countries with over 775,000 employees worldwide.


Business Unit

Life Sciences R&D – Pharmacovigilance Operations

The role is part of Accenture’s Life Sciences Research & Development division, supporting:

  • Clinical operations

  • Pharmacovigilance

  • Regulatory services

  • Patient safety solutions


Role Summary

The Pharmacovigilance Services New Associate will support end-to-end pharmacovigilance and drug safety operations, including:

  • Adverse Event (AE) processing

  • Individual Case Safety Report (ICSR) management

  • Medical coding

  • Safety database management

  • Regulatory submissions

  • Follow-up and reconciliation activities

The role focuses on ensuring compliance with client SOPs, regulatory timelines, and quality standards.


Key Responsibilities

ICSR & Case Processing

  • Prioritize and triage incoming safety cases

  • Create and manage cases in the global safety database

  • Review source documents for validity and completeness

  • Perform duplicate checks and case assessments

  • Process:

    • AEs (Adverse Events)

    • SAEs (Serious Adverse Events)

    • SUSARs (Suspected Unexpected Serious Adverse Reactions)

Medical Coding

  • Perform:

    • MedDRA coding

    • WHO-Drug coding

  • Code:

    • Medical history

    • Suspect drugs

    • Adverse events

Safety Evaluation & Documentation

  • Assess:

    • Seriousness

    • Causality

    • Medical significance

  • Draft:

    • Case narratives

    • E2B sender comments

  • Review and update follow-up information

Regulatory Compliance

  • Ensure compliance with:

    • Client SOPs

    • Global regulatory requirements

    • Submission timelines

  • Perform submissions through global safety databases

Follow-Up & Query Management

  • Request missing safety information

  • Send follow-up queries to reporters or marketing companies

  • Resolve pending action items and clarifications

Database & Documentation Management

  • Archive safety communications and documents

  • Monitor and reconcile client mailboxes

  • Handle case corrections and deletions

  • Support Trial Master File (TMF) review activities

Additional Responsibilities

  • Participate in:

    • Audits

    • Inspections

    • Pharmacovigilance projects

  • Prepare meeting minutes and agendas

  • Support cross-functional coordination

  • Perform translations where required

  • Conduct unblinding activities as per SOPs


Required Qualifications

Educational Qualification

  • Bachelor of Pharmacy (B.Pharm)

  • B.Sc. Nursing


Required Skills & Knowledge

Technical Skills

  • MS Office proficiency

  • Knowledge of safety databases

  • Familiarity with:

    • MedDRA

    • WHO-Drug Dictionary

Pharmacovigilance Knowledge

  • Understanding of:

    • Adverse Event reporting

    • ICSR processing

    • Drug safety surveillance

    • Regulatory timelines and compliance

Communication Skills

  • Strong English proficiency:

    • Reading

    • Writing

    • Listening

    • Speaking

  • Good medical writing skills


Key Performance Indicators (KPIs)

KPI Area

Expectation

Case Quality

Accurate safety case processing

Regulatory Compliance

Meet submission timelines

Productivity

Process cases within TAT/SLA

Learning Ability

Quickly adapt to new processes

Documentation

Maintain complete and accurate records


Work Environment

  • Team-based pharmacovigilance operations environment

  • Compliance-driven workflows

  • Rotational shifts may be required

  • Opportunity for role transitions based on business requirements


Desired Candidate Profile

Ideal candidates should have:

  • Strong attention to detail

  • Analytical thinking

  • Ability to manage repetitive operational tasks

  • Good organizational skills

  • Willingness to learn and adapt

  • Ability to work under timelines


Career Growth Opportunities

This role can lead to:

  • Drug Safety Associate

  • Senior Pharmacovigilance Associate

  • Safety Data Specialist

  • Medical Reviewer

  • Pharmacovigilance Analyst

  • Regulatory Affairs Associate


Diversity & Inclusion

Accenture promotes:

  • Equal employment opportunity

  • Inclusive workplace culture

  • Diversity and belonging

  • Employee well-being and continuous learning

Employment decisions are made without discrimination based on:

  • Race

  • Gender

  • Religion

  • Disability

  • Sexual orientation

  • Veteran status

  • Citizenship status

  • Other protected categories


Suitable For

This role is suitable for:

  • Freshers in pharmacy or nursing

  • Candidates interested in pharmacovigilance careers

  • Entry-level professionals seeking drug safety experience

  • Healthcare graduates interested in clinical research and regulatory operations