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Pharmacovigilance Services Associate

0-2 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
Position: Pharmacovigilance Services Associate
Employment Type: Full Time
Experience Required: 0 to 2 years (Entry Level)

Accenture is seeking motivated Pharmacovigilance Services Associates to support its global Drug Safety and Life Sciences operations. This role is ideal for early-career professionals looking to build expertise in pharmacovigilance, drug safety surveillance, and case processing within a leading multinational environment.


About the Role

You will work within Accenture’s Life Sciences R&D vertical, supporting end-to-end pharmacovigilance processes for global biopharmaceutical clients. This includes safety case intake, data management, quality review, and compliance with international regulatory standards.


Key Responsibilities

  • Manage affiliate mailbox activities, safety report intake, and reconciliation.

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

  • Execute ICSR case identification, data entry, MedDRA coding, processing, and submissions.

  • Ensure accuracy and compliance with client-specific guidelines and global pharmacovigilance regulations.

  • Maintain documentation and database activities in line with safety and quality standards.

  • Resolve routine issues by referencing established processes and guidelines.

  • Collaborate with team members and supervisors to meet operational milestones.

  • Work as an individual contributor with a clear and defined scope of work.

  • Be prepared to work in rotational shifts as required by project needs.


Required Experience

  • 0 to 2 years of experience in Pharmacovigilance, Drug Safety Operations, Clinical Data Management, or relevant Life Science domains.

  • Fresh graduates with strong foundational knowledge are encouraged to apply.


Educational Qualifications

Candidates must hold one of the following degrees:

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)


Required Skills

  • Knowledge of Pharmacovigilance Operations and Drug Safety Surveillance

  • Understanding of ICSR workflows and MedDRA coding

  • Strong written and verbal communication skills

  • Ability to follow standard operating procedures and regulatory requirements

  • Good analytical, documentation, and teamwork abilities


About Accenture

Accenture is a global professional services leader in digital, cloud, technology, and security. With expertise across more than 40 industries and one of the world’s largest intelligent operations networks, Accenture delivers innovation and value to clients across 120+ countries. The company combines advanced technology capabilities with human expertise to drive transformation and long-term success.