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Pharmacovigilance Services Associate

Accenture
Accenture
0-3 years
preferred by company
10 Jan. 7, 2026
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

Pharmacovigilance Services Associate

Company: Accenture
Location: Bengaluru, India
Employment Type: Full-Time
Job ID: AIOC-S01619343
Experience Required: 0–2 Years (Up to 3 years considered)
Industry: Pharmacovigilance | Drug Safety | Life Sciences R&D


Job Overview

Accenture is seeking a Pharmacovigilance Services Associate to join its Life Sciences R&D vertical in Bengaluru. This role offers an excellent opportunity for early-career professionals to build expertise in pharmacovigilance operations and drug safety surveillance, supporting global biopharmaceutical companies in ensuring patient safety and regulatory compliance.

As part of Accenture’s Clinical, Pharmacovigilance & Regulatory services, you will contribute to end-to-end safety case processing and pharmacovigilance activities aligned with global regulatory standards.


Key Responsibilities

  • Perform pharmacovigilance operations including case intake, case identification, and data entry for Individual Case Safety Reports (ICSRs).

  • Conduct MedDRA coding, case processing, submissions, and follow-ups in safety databases as per client SOPs and regulatory requirements.

  • Monitor, assess, and document adverse events (AEs) and other drug safety information from multiple data sources.

  • Ensure compliance with global pharmacovigilance regulations and internal quality standards.

  • Support routine safety surveillance activities related to clinical trials, post-marketing safety, and patient safety programs.

  • Work as an individual contributor within a defined scope while collaborating closely with team members and supervisors.

  • Follow established guidelines and procedures to resolve routine operational issues.

  • Maintain accurate documentation and meet productivity and quality benchmarks.

  • Be open to working in rotational shifts, as required by project needs.


Required Qualifications

  • Educational Qualification:

    • MSc (Life Sciences)

    • Bachelor of Pharmacy (B.Pharm)

    • Master of Pharmacy (M.Pharm)

  • Experience:

    • 0–2 years of experience in pharmacovigilance, drug safety, or life sciences operations

    • Candidates with up to 3 years of relevant experience may also be considered


Skills & Competencies

  • Basic understanding of pharmacovigilance and drug safety surveillance processes

  • Familiarity with ICSR processing, safety databases, and MedDRA terminology is preferred

  • Strong attention to detail and data accuracy

  • Ability to follow defined processes and regulatory guidelines

  • Good written and verbal communication skills

  • Ability to work effectively in a team-based, structured environment


About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, security, and life sciences operations. With a workforce of over 699,000 professionals across 120+ countries, Accenture helps organizations drive innovation and deliver measurable value through technology and human ingenuity.


Why Join This Role

  • Entry-level opportunity to build a career in pharmacovigilance and drug safety

  • Exposure to global life sciences and biopharma clients

  • Structured learning and process-driven work environment

  • Strong foundation for long-term growth in clinical research, regulatory affairs, and safety surveillance


Apply Now

If you are a pharmacy or life sciences graduate looking to start or grow your career in pharmacovigilance and drug safety operations, this role offers a strong platform to gain hands-on industry experience.