Accenture is a leading global professional services company with expertise in digital, cloud, and security. With unmatched experience across 40+ industries, Accenture provides Strategy & Consulting, Technology, Operations, and Accenture Song services. The company’s 699,000 professionals deliver cutting-edge solutions to clients in over 120 countries, driving innovation and business success.
🔗 Website: www.accenture.com
Job Description
As a Pharmacovigilance Services Associate, you will be part of Accenture’s Life Sciences R&D team, supporting pharmacovigilance and drug safety surveillance. Your role will involve:
- Managing the Affiliate Mailbox and reconciling reports.
- Conducting follow-ups for Serious (SUSAR) and Non-serious adverse event cases.
- Performing case identification, data entry, MedDRA coding, and case processing in safety databases.
- Ensuring compliance with global regulatory requirements (FDA, EMA, etc.).
- Collaborating with cross-functional teams to maintain pharmacovigilance standards.
Key Skills & Qualifications
✅ Educational Background: B.Pharmacy / B.Physiotherapy / BSc. Nursing
✅ Experience: 1-3 years in pharmacovigilance or drug safety (Freshers with relevant degrees may apply)
✅ Preferred Skills:
- Knowledge of MedDRA coding and ICSR (Individual Case Safety Report) processing
- Familiarity with Argus, ARISg, or other safety databases
- Strong attention to detail & ability to work in a team
- Adaptability and quick learning ability
Why Join Accenture?
✔ Global Exposure: Work with top pharmaceutical & biotech companies.
✔ Career Growth: Opportunities in pharmacovigilance, regulatory affairs, and clinical research.
✔ Learning & Development: Continuous upskilling in drug safety and compliance.
