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Pharmacovigilance Services Specialist

Accenture
Accenture
5-10 years
Not Disclosed
Bengaluru, India
10 April 24, 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

Pharmacovigilance Services Specialist (Medical Review & Safety Reporting)

Job Overview

A leading global life sciences organization is hiring a Pharmacovigilance Services Specialist responsible for medical review of aggregate safety reports and regulatory submissions. The role ensures compliance with global pharmacovigilance standards and supports patient safety through accurate drug safety surveillance and reporting.

Experience Required

7 to 11 years of experience in Pharmacovigilance, Drug Safety, or Medical Review roles.

Location

Bengaluru, India

Job Type

Full-time


Key Responsibilities

  • Perform medical review of aggregate safety reports including PBRER/PSUR and Risk Management Plans (RMP).

  • Ensure accuracy, completeness, and compliance with global regulatory and client-specific SOPs.

  • Oversee case processing activities including case intake, MedDRA coding, data entry, and ICSR submissions.

  • Conduct follow-ups and ensure timely reporting of safety cases in global safety databases.

  • Contribute to pharmacovigilance system compliance and inspection readiness.

  • Collaborate with cross-functional teams to ensure high-quality safety deliverables.

  • Support continuous improvement initiatives in pharmacovigilance operations.


Required Skills and Expertise

  • Strong experience in PBRER/PSUR authoring and review.

  • Expertise in Pharmacovigilance Operations and Drug Safety Surveillance.

  • Knowledge of global regulatory guidelines and compliance frameworks.

  • Experience with adverse event reporting and safety databases.

  • Strong analytical and medical writing skills.

  • Ability to manage complex safety datasets and regulatory documentation.


Preferred Qualifications

  • Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm) / BSc Nursing.

  • Strong understanding of pharmacovigilance lifecycle and regulatory reporting requirements.


Key Competencies

  • Medical review and scientific evaluation

  • Regulatory compliance and safety reporting

  • Attention to detail and analytical thinking

  • Stakeholder management and collaboration

  • Ability to work in rotational shifts

  • Problem-solving in moderately complex pharmacovigilance cases


About the Role

This position plays a critical role in ensuring global patient safety by managing pharmacovigilance reporting activities and delivering high-quality regulatory safety documentation. The role contributes directly to global drug safety compliance and supports pharmaceutical product lifecycle monitoring.


Pharmacovigilance Industry Focus

  • Drug Safety Monitoring

  • Aggregate Reporting (PSUR/PBRER)

  • Regulatory Compliance

  • Clinical Safety Evaluation

  • Medical Data Review