Accenture is seeking a Pharmacovigilance Services New Associate to join their Life Sciences R&D team in Bengaluru. This role is ideal for fresh graduates or professionals with up to 2 years of experience in pharmacovigilance and drug safety surveillance.
Key Responsibilities:
- Manage the Affiliate Mailbox and perform case reconciliation.
- Conduct follow-ups for both serious and non-serious adverse event reports.
- Identify, enter, and process Individual Case Safety Reports (ICSRs) in the safety database.
- Ensure accurate MedDRA coding and compliance with global regulatory requirements.
- Collaborate with internal teams and adhere to client-specific pharmacovigilance guidelines.
- Work in rotational shifts as per business needs.
Skills & Qualifications:
- Bachelor of Pharmacy (B.Pharm) is mandatory.
- 0-1 year of experience in pharmacovigilance, drug safety, or clinical research.
- Strong attention to detail and ability to follow standard operating procedures (SOPs).
- Proficiency in English (Advanced level) for documentation and communication.
- Basic understanding of pharmacovigilance regulations (GVP, ICH-GCP, FDA, EMA) is a plus.
About Accenture
Accenture is a global leader in professional services, specializing in digital, cloud, and security solutions. With a workforce of over 699,000 professionals across 120+ countries, Accenture delivers cutting-edge services in Strategy & Consulting, Technology, Operations, and Accenture Song.
The Life Sciences R&D vertical focuses on pharmacovigilance, clinical trials, regulatory affairs, and patient safety, helping biopharma companies enhance patient outcomes through innovation and compliance.
Why Join Accenture?
✅ Work with a Fortune 500 company and global industry leaders.
✅ Gain exposure to pharmacovigilance case processing and regulatory compliance.
✅ Opportunities for career growth and skill development.
✅ Rotational shifts with structured training and mentorship.
