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Pharmacovigilance Services Associate

Accenture
Accenture
0-2 years
Not Disclosed
10 Dec. 22, 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

Title: Pharmacovigilance Services Associate – Bengaluru, India
Location: Bengaluru, India
Job Type: Full-Time
Category: Pharmacovigilance / Drug Safety

Company Overview:
Accenture is a global professional services leader with unmatched expertise in digital, cloud, and security solutions. Operating across 40+ industries, Accenture combines technology with human ingenuity to help clients improve outcomes, drive innovation, and solve complex challenges. With 699,000 professionals in 120+ countries, Accenture empowers people and organizations to create lasting value.

Role Overview:
We are seeking a Pharmacovigilance Services Associate to support drug safety operations within the Life Sciences R&D vertical. This role focuses on monitoring and assessing the safety of pharmaceutical products, detecting, evaluating, and preventing adverse effects, and ensuring compliance with global regulatory requirements.

Key Responsibilities:

  • Collect, process, and analyze safety data from clinical trials, healthcare providers, and patients.

  • Manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for Individual Case Safety Reports (ICSRs) in the safety database per client guidelines.

  • Solve routine pharmacovigilance problems using established guidelines and protocols.

  • Interact with internal team members and supervisors to ensure accurate, timely safety reporting.

  • Maintain adherence to applicable global regulatory standards and SOPs.

  • Work in rotational shifts as required to meet operational demands.

Qualifications & Experience:

  • Education: MSc, BPharm, or MPharm in a relevant life sciences discipline.

  • Experience: 0–2 years in pharmacovigilance or drug safety operations.

  • Familiarity with ICSR processes, MedDRA coding, and safety databases is advantageous.

Skills & Competencies:

  • Strong attention to detail and analytical skills.

  • Knowledge of medical terminology and pharmacovigilance processes.

  • Good time management and multi-tasking abilities.

  • Effective communication skills and ability to work collaboratively in a team.

  • Ability to follow guidelines and resolve routine issues with minimal supervision.

Why Join Accenture:

  • Opportunity to work in a globally recognized organization at the forefront of digital and life sciences innovation.

  • Access to continuous learning and professional development programs.

  • Inclusive and diverse work environment fostering collaboration and creativity.

  • Competitive compensation and benefits package.

Equal Opportunity Employer:
Accenture provides equal employment opportunities to all applicants without regard to age, race, gender, religion, disability, veteran status, sexual orientation, or any legally protected status.

Apply Today: Join Accenture to advance your career in pharmacovigilance and drug safety, contributing to safer medicines and improved patient outcomes globally.