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Pharmacovigilance Services Specialist

Accenture
7-11 years
INR 15 LPA – 25 LPA
Bangalore, India
1 June 12, 2026
Job Description
Job Type: Full Time Education: MBBS Skills: CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

Job Title: Pharmacovigilance Services Specialist
Company: Accenture
Location: Bengaluru
Job Type: Full-Time
Experience Required: 7–11 Years
Qualification: MBBS

About the Role
Accenture is hiring a Pharmacovigilance Services Specialist to provide medical review, safety assessment, pharmacovigilance oversight, and clinical expertise for global drug safety operations. The role involves reviewing ICSRs, evaluating adverse events, performing medical assessments, mentoring teams, supporting audits, and ensuring compliance with global pharmacovigilance regulations and client requirements.

Key Responsibilities

Medical Review & Safety Assessment

  • Review Individual Case Safety Reports (ICSRs) for medical accuracy and completeness.

  • Assess adverse events for seriousness, causality, expectedness, and clinical significance.

  • Review MedDRA coding, labeling information, and medical narratives.

  • Provide medical assessment comments and recommendations for case processing.

Case Quality & Compliance

  • Ensure consistency between source documents, narratives, coding, and safety assessments.

  • Verify that all relevant clinical information is presented in a logical chronological sequence.

  • Review case quality and ensure compliance with client SOPs and global regulations.

  • Route cases for corrections when quality issues are identified.

Case Follow-Up & Workflow Management

  • Prioritize medical review activities according to SLAs, KPIs, and turnaround timelines.

  • Initiate and review follow-up requests for missing or incomplete safety information.

  • Ensure timely case closure, routing, distribution, and database locking activities.

  • Support case processing teams in resolving medical and regulatory queries.

Stakeholder & Client Support

  • Participate in client discussions and provide subject matter expertise.

  • Support regulatory inspections, audits, and compliance activities.

  • Collaborate with case processing, quality review, and data entry teams.

  • Act as a medical escalation point for complex safety cases.

Training & Mentorship

  • Train, mentor, and guide junior pharmacovigilance associates.

  • Provide feedback to operational teams to improve data quality and compliance.

  • Support knowledge-sharing initiatives and continuous process improvements.

  • Stay updated on global pharmacovigilance regulations and industry best practices.

Required Skills

  • Medical Review of ICSRs

  • Pharmacovigilance & Drug Safety

  • Adverse Event Assessment

  • MedDRA Coding Review

  • Medical Narrative Review

  • Clinical Risk Assessment

  • Signal Detection Support

  • Global Pharmacovigilance Regulations

  • Quality & Compliance Management

  • Audit & Inspection Readiness

  • Stakeholder Management

  • Team Mentoring & Training

Preferred Qualifications

  • Experience in medical review and pharmacovigilance operations within CRO, pharmaceutical, or healthcare organizations.

  • Strong knowledge of FDA, EMA, MHRA, ICH, and GVP guidelines.

  • Experience with Argus Safety, ArisG, PV-Works, or similar safety databases.

  • Exposure to aggregate reports, signal management, and benefit-risk evaluation.

  • Experience supporting regulatory inspections and client audits.