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Pharmacovigilance Services Associate

Accenture
Accenture
1-3 years
Not Disclosed
10 Nov. 25, 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

Location: Multiple Locations
Employment Type: Full-Time
Experience Required: 1 to 3 years
Qualification: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm)


About the Role

Accenture is seeking a Pharmacovigilance Services Associate to support its expanding Life Sciences R&D operations. This role focuses on Pharmacovigilance Operations, specifically Pharmacovigilance and Drug Safety Surveillance, contributing to high-quality safety data management and compliance with global regulatory standards.

You will be part of Accenture’s Life Sciences R&D vertical, supporting leading biopharmaceutical organizations across research, clinical development, regulatory services, and patient safety functions. This position plays a crucial role in strengthening drug safety processes and improving patient outcomes.


Key Responsibilities

  • Manage safety case identification, data entry, MedDRA coding, case processing, submissions, and follow-ups for ICSRs in accordance with client guidelines and global regulatory requirements.

  • Oversee Affiliate Mailbox activities, including report reconciliation and follow-up of Serious and Non-Serious adverse event cases.

  • Apply standardized processes and established precedents to resolve routine operational challenges.

  • Collaborate within the team and engage with direct supervisors for task execution and issue resolution.

  • Execute daily tasks with detailed instructions, while following structured workflows for new assignments.

  • Work as an individual contributor within a focused domain of Pharmacovigilance Operations.

  • Be available for rotational shift work based on project needs.


Required Skills and Experience

  • 1 to 3 years of experience in Pharmacovigilance, Drug Safety Operations, or related life sciences functions.

  • Strong understanding of global pharmacovigilance regulations and safety reporting requirements.

  • Hands-on experience with MedDRA coding, safety databases, and ICSR case processing.

  • Effective communication and documentation skills within cross-functional teams.

  • Ability to follow standard operating procedures and maintain compliance-driven workflows.


About Accenture

Accenture is a global professional services leader, delivering industry-leading expertise in digital, cloud, security, consulting, technology, and operations. With a workforce of over 699,000 professionals across more than 120 countries, Accenture partners with organizations to drive innovation, create value, and transform operations.

For more information, visit the Accenture website.