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Pharmacovigilance Services Associate

Fresher years
3-5 LPA
15 Dec. 2, 2025
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Lifesciences graduate 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 | Chennai, India

Job Type: Full-Time
Experience Required: 0–2 years (Freshers Eligible)
Expected Salary Range: ₹3.0 LPA – ₹5.5 LPA (based on skills and experience)
Job ID: AIOC-S01615695


About the Role

Accenture is hiring Pharmacovigilance Services Associates to support global drug safety operations within its Life Sciences R&D vertical. This role offers hands-on exposure to case processing, adverse event assessment, and regulatory compliance, making it an excellent opportunity for freshers and early-career professionals looking to build expertise in pharmacovigilance and drug safety surveillance.

You will work within Accenture’s Clinical, Pharmacovigilance & Regulatory services team, supporting top biopharma clients in end-to-end safety case management, patient-level data review, and follow-up coordination as per global regulatory guidelines.


Key Responsibilities

  • Perform case intake, case identification, and triage in alignment with client procedures.

  • Conduct data entry, MedDRA coding, case processing, narrative creation, and regulatory submission support for ICSRs.

  • Manage affiliate mailbox activities, including report reconciliation and documentation of all follow-up actions for serious and non-serious cases.

  • Ensure compliance with global regulatory requirements, client SOPs, and pharmacovigilance quality standards.

  • Perform written follow-ups for missing information and maintain accurate case tracking.

  • Collaborate with internal teams and supervisors to ensure timely completion of assigned tasks.

  • Work within well-defined guidelines and escalate complex issues when required.

  • Support continuous quality improvement in safety data management.

  • Be willing to work in rotational shifts as per business needs.


Skills & Competencies Required

  • Strong understanding of pharmacovigilance concepts and ICSR lifecycle.

  • Knowledge of MedDRA coding, safety database workflows, and global reporting timelines.

  • Good analytical ability to review and interpret clinical information.

  • Strong written and verbal communication skills.

  • Ability to follow structured processes with high attention to detail.

  • Team-oriented mindset with the ability to work as an individual contributor.


Education Requirement

  • Bachelor of Pharmacy (B.Pharm) is mandatory.


About Accenture

Accenture is a global professional services leader with deep expertise in digital transformation, cloud technologies, security, operations, consulting, and intelligent business solutions. With more than 699,000 employees across 120+ countries, Accenture partners with leading organizations to drive innovation and deliver measurable impact across more than 40 industries.
Learn more at: www.accenture.com


Location

Chennai, India