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Pharmacovigilance Services New Associate

Accenture
Accenture
0-2 years
Not Disclosed
Bengaluru, India
10 March 10, 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

Job Title: Pharmacovigilance Services New Associate
Company: Accenture
Location: Bengaluru, India
Job Type: Full-Time
Experience Required: 0–2 Years
Job ID: AIOC-S01630790

About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud, and security. The organization combines extensive industry experience with specialized expertise across more than 40 industries, delivering services in Strategy and Consulting, Technology, and Operations, along with Accenture Song. With a workforce of over 784,000 professionals and a global network of Advanced Technology and Intelligent Operations Centers, Accenture serves clients in more than 120 countries. The company focuses on innovation and transformation to help organizations create long-term value and improve business performance.

Role Overview
Accenture is seeking a Pharmacovigilance Services New Associate to join its Life Sciences Research and Development (R&D) division in Bengaluru. This role supports pharmacovigilance operations and drug safety surveillance activities for global pharmaceutical and biotechnology clients. The selected candidate will contribute to monitoring the safety of pharmaceutical products, ensuring regulatory compliance, and supporting drug safety reporting processes.

Key Responsibilities

Pharmacovigilance Case Processing

  • Perform case identification and manage safety case data entry in pharmacovigilance databases.

  • Conduct MedDRA coding and maintain accurate safety data records.

  • Process Individual Case Safety Reports (ICSRs) in accordance with client guidelines and global regulatory requirements.

  • Support safety case submission and follow-up activities within required timelines.

Drug Safety Surveillance

  • Monitor and assess adverse events and drug-related safety data.

  • Assist in evaluating potential safety signals and maintaining accurate pharmacovigilance records.

  • Ensure compliance with global pharmacovigilance standards and regulatory frameworks.

Data Management and Compliance

  • Maintain quality and accuracy in safety data documentation and case processing.

  • Follow internal standard operating procedures and regulatory guidelines.

  • Support documentation and reporting activities required for pharmacovigilance operations.

Team Collaboration and Operational Support

  • Work closely with team members and supervisors to ensure efficient case processing.

  • Follow established workflows and operational procedures within the pharmacovigilance team.

  • Contribute as an individual team member supporting routine pharmacovigilance tasks.

Work Environment

  • This role involves handling structured and routine pharmacovigilance processes.

  • Employees may be required to work in rotational shifts depending on project requirements.

  • Tasks will be performed under supervision with clearly defined operational guidelines.

Educational Qualifications

  • Master of Science (MSc) in Life Sciences or a related discipline

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)

Experience Requirements

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

  • Fresh graduates with relevant academic knowledge in pharmacovigilance and drug safety are encouraged to apply.

Required Skills and Competencies

  • Basic understanding of pharmacovigilance operations and drug safety surveillance.

  • Knowledge of adverse event reporting and safety case processing concepts.

  • Familiarity with MedDRA coding and ICSR management is advantageous.

  • Strong attention to detail and analytical thinking.

  • Good communication and teamwork skills.

Job Location
Bengaluru, India.