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Pharmacovigilance Services Associate – Accenture

0-2 years
upto 5 LPA
10 Nov. 18, 2025
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. 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

Pharmacovigilance Services Associate – Accenture | Bengaluru, India

Job Code: AIOC-S01613990
Position Type: Full-Time
Experience Required: Fresher (0–2 years)

About the Role

Accenture is hiring Pharmacovigilance Services Associates to support global drug safety operations within its Life Sciences R&D vertical. This role is designed for freshers who want to build a career in Pharmacovigilance, Drug Safety Surveillance, and ICSR case processing for leading biopharma clients.

As part of Accenture’s Clinical, Pharmacovigilance and Regulatory services team, you will contribute to end-to-end safety operations including case intake, medical coding, report submission, and compliance with global regulatory guidelines.


Key Responsibilities

  • Manage Affiliate Mailbox activities, including receipt, triage, and reconciliation of safety reports.

  • Perform written follow-up for both serious and non-serious cases as per client procedures.

  • Create, process, and manage ICSRs in the safety database following global regulatory requirements.

  • Conduct case identification, data entry, MedDRA coding, narrative writing, consistency checks, and timely submission.

  • Apply client guidelines, SOPs, and pharmacovigilance standards for quality case processing.

  • Maintain accurate documentation and ensure compliance with regulatory timelines.

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

  • Follow detailed instructions for daily tasks and new assignments while adhering to established processes.

  • Collaborate within your team and consult your supervisor for guidance.

  • Support routine operations and deliver high-quality safety surveillance activities.

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


Required Skills

  • Strong interest in Pharmacovigilance, Drug Safety Surveillance, and ICSR processing.

  • Ability to follow structured workflows and established guidelines.

  • Good communication and documentation skills.

  • Familiarity with MedDRA terminology is an advantage.

  • High attention to detail and accuracy.

  • Ability to work effectively in a team and manage assigned tasks independently.

  • Strong analytical approach to routine problem-solving.


Education

  • Bachelor of Pharmacy (B.Pharm) or

  • Master of Pharmacy (M.Pharm)


About Accenture

Accenture is a global professional services leader with expertise in digital, cloud, and security solutions. With operations in more than 120 countries and a workforce of over 699,000 professionals, Accenture delivers strategy, consulting, technology, and operations services across 40+ industries. The Life Sciences R&D vertical supports research, clinical development, regulatory operations, and pharmacovigilance services for global biopharma organizations.


Location

Bengaluru, India