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Pharmacovigilance Services New Associate

Accenture
Accenture
0-2 years
Not Disclosed
Bengaluru, Karnataka, India
10 Feb. 17, 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 New Associate

Location: Bengaluru, Karnataka, India
Job Type: Full-Time
Experience Required: 0–2 Years
Job ID: AIOC-S01628146
Industry: Life Sciences / Pharmacovigilance / Drug Safety

Company Overview
Accenture is a global professional services organization specializing in digital, cloud, and security solutions, with extensive expertise across more than 40 industries. The company delivers services in strategy, consulting, technology, and operations through a global network of advanced technology and intelligent operations centers. With operations in over 120 countries, Accenture supports organizations in driving innovation, improving operational efficiency, and delivering sustainable value through technology and human ingenuity.

Role Overview
The Pharmacovigilance Services New Associate will support pharmacovigilance operations within the Life Sciences Research and Development vertical. This role focuses on drug safety surveillance, case processing, and regulatory compliance activities to ensure the safety and effectiveness of pharmaceutical products. The position contributes to monitoring adverse drug reactions, maintaining safety databases, and supporting global pharmacovigilance requirements.

This is an entry-level opportunity designed for professionals seeking to build expertise in drug safety, regulatory compliance, and pharmacovigilance operations.

Key Responsibilities

  • Support pharmacovigilance operations including drug safety surveillance and adverse event monitoring.

  • Perform case identification, data entry, and case processing in safety databases.

  • Conduct MedDRA coding and manage Individual Case Safety Reports (ICSRs).

  • Ensure accurate submission and follow-up of safety cases in accordance with global regulatory requirements and client guidelines.

  • Monitor and evaluate adverse drug reactions and safety-related information from clinical trials, healthcare providers, and patients.

  • Maintain compliance with pharmacovigilance processes and regulatory standards.

  • Resolve routine operational tasks based on established procedures and guidelines.

  • Collaborate with team members and supervisors to ensure quality and timely deliverables.

  • Work as an individual contributor within a structured team environment.

  • Support operational requirements including rotational shift schedules where applicable.

Required Skills and Competencies

  • Knowledge of pharmacovigilance operations and drug safety processes.

  • Understanding of adverse event reporting and safety data management.

  • Basic awareness of global regulatory standards in pharmacovigilance.

  • Strong analytical and documentation skills.

  • Attention to detail and process-oriented approach.

  • Ability to work in a collaborative team environment.

Educational Qualifications

  • Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm), BSc, or MSc in Life Sciences or related disciplines.

Experience Requirements

  • 0–2 years of experience in pharmacovigilance, drug safety, or related life sciences functions.

  • Fresh graduates with relevant academic background may apply.

Work Environment

  • Structured operational role with defined processes and supervision.

  • Opportunity to gain hands-on experience in global pharmacovigilance operations.

  • Rotational shift work may be required based on project needs.

Career Growth Opportunities
This role provides exposure to global pharmacovigilance practices, regulatory compliance frameworks, and drug safety operations, offering strong career progression opportunities within life sciences and healthcare services.