Instagram
youtube
Facebook

Pharmacovigilance Services Associate

1–3 years years
Not Disclosed
10 Sept. 2, 2025
Job Description
Job Type: Full Time Education: Bachelor of Pharmacy (B.Pharm) 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 Associate

Job ID: AIOC-S01597707
Location: Chennai, India
Job Type: Full-Time
Experience Required: 1–3 years


About Accenture

Accenture is a global professional services company with expertise in digital, cloud, and security. With over 699,000 employees in more than 120 countries, Accenture delivers services in Strategy & Consulting, Technology, Operations, and Accenture Song—all supported by the world’s largest network of Advanced Technology and Intelligent Operations centers.

🔗 Visit: www.accenture.com


About the Role

As a Pharmacovigilance Services Associate, you will support the Life Sciences R&D vertical at Accenture, specifically within the Pharmacovigilance & Drug Safety Surveillance domain. You'll be involved in case management, report reconciliation, and follow-up activities for adverse events, ensuring compliance with global regulatory requirements.


Key Responsibilities

  • Manage the Affiliate Mailbox for pharmacovigilance case intake.

  • Perform reconciliation of reports in accordance with defined processes.

  • Execute written follow-up for Serious and Non-serious Adverse Events (AEs).

  • Conduct case identification, data entry, and MedDRA coding.

  • Handle case processing, ICSR submissions, and follow-ups in the safety database.

  • Ensure compliance with client-specific guidelines and global regulatory standards.

  • Collaborate with cross-functional teams in the Clinical, Pharmacovigilance & Regulatory domain.


Required Qualifications

  • Educational Background:

    • Bachelor of Pharmacy (B.Pharm)

  • Experience:

    • 1 to 3 years in Pharmacovigilance or related drug safety roles


Skills and Attributes

  • Sound knowledge of pharmacovigilance processes and regulatory compliance

  • Proficient in MedDRA coding, ICSR processing, and using safety databases

  • Strong written and verbal communication skills

  • High attention to detail and analytical mindset

  • Ability to follow structured guidelines and adapt to evolving client needs


Work Environment

You will work within Accenture's Life Sciences R&D vertical, which supports biopharma companies across areas like:

  • Research labs

  • Clinical trial support

  • Regulatory services

  • Pharmacovigilance

  • Patient services

You will contribute to helping clients improve patient outcomes by combining scientific expertise with real-world insights.


What Accenture Offers

  • Opportunities to work on transformational projects in the healthcare and life sciences industry

  • Access to leading technologies and industry experts

  • Career development and learning pathways through continuous training

  • A supportive and inclusive work culture


Application Instructions

🔗 Apply Now via Accenture Careers


Learn More

  • Learn About Accenture's Hiring Process

  • Interview Preparation Tips

  • Explore Benefits at Accenture


Diversity & Inclusion

Accenture is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment regardless of race, gender, age, disability, sexual orientation, or religion.