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Pharmacovigilance Services Associate

Accenture
1-3 years
₹4.5 LPA – ₹7 LPA
Bangalore, India
15 July 8, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Services Associate

Company: Accenture
Location: Bengaluru, India
Job Requisition ID: AIOC-S01653592
Employment Type: Full-Time


Job Summary

Accenture is hiring a Pharmacovigilance Services Associate to support global drug safety and pharmacovigilance operations. The role involves ICSR case processing, MedDRA coding, safety data entry, adverse event management, case submissions, and follow-up activities while ensuring compliance with global pharmacovigilance regulations and client requirements.


Key Responsibilities

  • Identify and process Individual Case Safety Reports (ICSRs).

  • Perform safety data entry into pharmacovigilance databases.

  • Conduct MedDRA coding for adverse events and medical terms.

  • Review and process drug safety cases according to client guidelines.

  • Submit ICSRs within global regulatory timelines.

  • Perform case follow-up activities to obtain missing information.

  • Ensure compliance with pharmacovigilance SOPs and regulatory requirements.

  • Maintain accurate documentation of safety cases.

  • Support adverse event monitoring and drug safety surveillance.

  • Collaborate with internal teams to ensure timely case processing.

  • Resolve routine pharmacovigilance issues by following established guidelines.

  • Perform assigned activities while maintaining quality and productivity targets.

  • Work in rotational shifts as required.


Required Skills

  • Pharmacovigilance (PV)

  • Drug Safety

  • ICSR Case Processing

  • Adverse Event Reporting

  • MedDRA Coding

  • Safety Data Entry

  • Safety Database Management

  • Case Processing

  • Regulatory Submissions

  • Drug Safety Surveillance

  • Clinical Research

  • Medical Terminology

  • SOP Compliance

  • Quality Documentation

  • Attention to Detail

  • Communication Skills

  • Time Management

  • Microsoft Office


Eligibility

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)


Experience

Required Experience: 1–3 years of experience in Pharmacovigilance, Drug Safety, ICSR Case Processing, or Clinical Safety Operations.


Salary Package (Estimated Market Standard)

₹4.5 LPA – ₹7 LPA (depending on experience, pharmacovigilance expertise, and interview performance).


Work Mode

  • Full-Time

  • Bengaluru Location

  • Rotational Shifts


Why Join Accenture?

  • Opportunity to work with leading global pharmaceutical and biotechnology companies.

  • Exposure to global pharmacovigilance and drug safety operations.

  • Career growth through structured learning and certification programs.

  • Collaborative and technology-driven work environment.

  • Access to advanced digital, cloud, and AI-powered healthcare solutions.

  • Global career opportunities within Accenture's Life Sciences division.


About Accenture

Accenture is a leading global professional services company specializing in Strategy & Consulting, Technology, Operations, Industry X, and Song. With approximately 791,000 employees across more than 120 countries, Accenture helps organizations transform through digital technologies, cloud computing, artificial intelligence, and data-driven solutions. Within its Life Sciences R&D division, Accenture supports pharmaceutical and biotechnology companies across clinical research, regulatory affairs, pharmacovigilance, and patient services, helping accelerate innovation and improve patient outcomes.