Accenture is hiring Pharmacovigilance Services New Associate professionals in Bengaluru, India. This opportunity is ideal for MSc and M.Pharm graduates with 0–1 year experience who want to start their career in pharmacovigilance, drug safety surveillance, and life sciences operations.
The role is part of Accenture’s Life Sciences R&D vertical, where professionals support global biopharmaceutical companies in clinical research, pharmacovigilance operations, regulatory compliance, and patient safety monitoring.
Candidates interested in drug safety associate roles, pharmacovigilance operations, and clinical safety data processing should consider this entry-level opportunity.
Job Overview
- Position: Pharmacovigilance Services New Associate
- Department: Pharmacovigilance Operations – Drug Safety
- Company: Accenture
- Location: Bengaluru, India
- Experience: 0 – 1 Year
- Qualification: MSc / Master of Pharmacy (M.Pharm)
- Employment Type: Full-time
This role involves working with pharmacovigilance teams responsible for monitoring drug safety, evaluating adverse events, and ensuring regulatory compliance for pharmaceutical products worldwide.
Key Responsibilities
The Pharmacovigilance Services New Associate will support drug safety and pharmacovigilance activities including:
- Case identification and ICSR case processing
- Safety data entry and management in pharmacovigilance databases
- MedDRA coding for adverse event reporting
- Processing Individual Case Safety Reports (ICSRs)
- Managing follow-ups for adverse event cases
- Supporting drug safety surveillance operations
- Ensuring compliance with global regulatory guidelines
- Working with clinical trial safety data and post-marketing safety reports
- Collaborating with pharmacovigilance teams and supervisors
The role focuses on routine pharmacovigilance tasks under supervision, making it suitable for fresh graduates entering drug safety careers.
Required Qualifications
Candidates applying for the Accenture Pharmacovigilance New Associate role must meet the following requirements:
- MSc (Life Sciences) OR Master of Pharmacy (M.Pharm)
- 0–1 year experience in pharmacovigilance or drug safety
- Strong understanding of drug safety reporting and adverse event management
- Familiarity with ICSR processing and MedDRA terminology
- Ability to analyze clinical safety data
- Good communication and teamwork skills
- Willingness to work in rotational shifts
Preferred Skills
- Knowledge of pharmacovigilance workflows
- Understanding of global drug safety regulations
- Experience with safety databases (Argus, ArisG, Veeva Safety etc.)
- Attention to detail in safety case processing
Why Join Accenture?
Working at Accenture offers strong career growth in life sciences operations and pharmacovigilance services.
Key benefits include:
- Exposure to global pharmaceutical safety projects
- Opportunities to work with leading biopharma companies
- Career growth in drug safety and regulatory operations
- Training in pharmacovigilance systems and compliance
- Global work environment with advanced digital technologies
About Accenture
Accenture is a global professional services company with strong capabilities in digital transformation, cloud computing, AI, and life sciences services.
With 790,000+ employees serving clients across 120+ countries, Accenture helps organizations accelerate innovation and deliver technology-driven solutions in industries including healthcare, pharmaceuticals, and clinical research.
How to Apply
