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Job Title: Pharmacovigilance Services Associate
Job Type: Full Time
Experience: 1–3 Years (freshers can apply)
Job ID: AIOC-S01597433
Location: Chennai
Job Overview
Accenture is seeking enthusiastic and detail-oriented Pharmacovigilance Services Associates to join its Life Sciences R&D vertical. This role is a great opportunity for fresh B.Pharm graduates or professionals with up to 2 years of experience to work with some of the world’s leading biopharma companies in ensuring drug safety, regulatory compliance, and patient well-being.
About Accenture
Accenture is a global professional services leader with expertise in digital, cloud, and security solutions. Operating in over 120 countries with a workforce of 699,000, the company partners with clients to drive innovation, improve performance, and deliver value. In the Life Sciences R&D division, Accenture works across research, clinical trials, regulatory affairs, pharmacovigilance, and patient support services.
Key Responsibilities
- Manage case identification, data entry, MedDRA coding, and case processing for drug safety.
- Handle ICSR (Individual Case Safety Report) submissions and follow-ups in the safety database.
- Manage affiliate mailbox and reconcile reports according to process guidelines.
- Ensure compliance with client-specific and global regulatory requirements.
- Conduct written follow-up attempts for serious and non-serious cases.
Qualifications & Skills Required
- Education: Bachelor of Pharmacy (B.Pharm)
- Experience: 1 to 3 years (pharmacovigilance experience preferred)
- Skills:
- Understanding of pharmacovigilance and drug safety surveillance
- Proficiency in MedDRA coding and safety database operations
- Strong attention to detail
- Ability to work within regulatory frameworks
Why Join Accenture?
- Work with global biopharma leaders
- Be part of a technology-driven, patient-focused healthcare environment
- Opportunities for professional growth and skill enhancement in the pharmaceutical industry
