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Pharmacovigilance Services Associate

1-3 years
Not Disclosed
10 Dec. 2, 2025
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 – Accenture | Bengaluru, India

Job ID: AIOC-S01614372
Location: Bengaluru, India
Role: Pharmacovigilance Services Associate
Employment Type: Full Time
Experience Required: 1 to 3 years

Accenture is hiring skilled Pharmacovigilance Services Associates to support its global Life Sciences and Drug Safety operations. This role is suited for life science graduates with foundational experience in pharmacovigilance, case processing, or drug safety surveillance.


About the Role

As part of Accenture’s Life Sciences R&D vertical, you will support critical safety operations across pharmacovigilance, regulatory services, and patient-centric solutions. You will work with leading biopharma clients to ensure the accurate capture, processing, and submission of safety data in alignment with global regulatory guidelines.


Key Responsibilities

  • Manage affiliate mailbox activities, including intake and reconciliation of safety reports.

  • Perform written follow-up for both serious and non-serious adverse event cases.

  • Handle case identification, ICSR data entry, MedDRA coding, case processing, quality checks, and timely submissions.

  • Ensure compliance with client-specific processes and global regulatory requirements.

  • Support safety database operations, documentation, and case management workflows.

  • Solve routine issues using established procedures and escalate when needed.

  • Collaborate closely with team members and supervisors to meet delivery expectations.

  • Work as an individual contributor with a defined scope of responsibilities.

  • Be prepared to work in rotational shifts based on project needs.


Required Experience

  • 1 to 3 years of experience in Pharmacovigilance, Drug Safety Operations, Clinical Data Management, or related life science domains.

  • Fresh graduates with strong foundational knowledge may be considered for entry-level opportunities.


Educational Qualifications

Applicants must hold one of the following degrees:

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)


Required Skills

  • Pharmacovigilance Operations

  • Drug Safety Surveillance

  • ICSR Case Processing

  • MedDRA Coding

  • Strong written communication and documentation abilities

  • Ability to follow structured processes and standard operating procedures


About Accenture

Accenture is a global professional services leader specializing in digital, cloud, technology, and security solutions. With expertise across 40+ industries and a network of advanced operations centers worldwide, Accenture delivers transformative value to clients in more than 120 countries through innovation, technology, and human ingenuity.