Accenture is hiring for the position of Pharmacovigilance Services Associate in Bengaluru, Karnataka. This is an excellent opportunity for B.Pharm and M.Pharm graduates with 1โ3 years of Pharmacovigilance experience who are looking to build their career in drug safety, ICSR case processing, MedDRA coding, and pharmacovigilance operations.
If you have experience in adverse event case processing, safety databases, regulatory compliance, and pharmacovigilance operations, this opportunity at Accenture can help you work with leading global pharmaceutical companies while contributing to patient safety.
Job Overview
- Company: Accenture
- Role: Pharmacovigilance Services Associate
- Job ID: AIOC-S01656900
- Location: Bengaluru, Karnataka
- Department: Pharmacovigilance Operations
- Employment Type: Full-Time
- Experience: 1โ3 Years
- Qualification: Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm)
About Accenture
Accenture is one of the world’s leading professional services companies, serving clients in over 120 countries. With expertise in digital, cloud, AI, consulting, and operations, Accenture supports global pharmaceutical organizations across clinical research, regulatory affairs, pharmacovigilance, and patient safety.
Within the Life Sciences R&D business, employees contribute to improving healthcare outcomes by supporting drug development, safety surveillance, and regulatory compliance.
Key Responsibilities
As a Pharmacovigilance Services Associate, your responsibilities will include:
- Perform end-to-end ICSR case processing.
- Identify and validate adverse event cases.
- Enter safety data into pharmacovigilance databases.
- Perform MedDRA coding accurately.
- Conduct medical case assessment as per SOPs.
- Submit cases according to global regulatory timelines.
- Follow up for missing safety information.
- Ensure compliance with client-specific guidelines.
- Maintain data quality and regulatory compliance.
- Support pharmacovigilance operations for global pharmaceutical clients.
- Collaborate with internal quality and safety teams.
- Complete assigned work within defined turnaround times.
Required Qualifications
Applicants should possess:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
Experience Required
- 1โ3 years of Pharmacovigilance experience.
- Experience in ICSR case processing.
- Knowledge of pharmacovigilance workflows.
- Familiarity with MedDRA coding.
- Experience working with safety databases is preferred.
- Understanding of global pharmacovigilance regulations.
Desired Skills
Candidates with the following skills will have an advantage:
- Pharmacovigilance Operations
- Drug Safety Surveillance
- ICSR Processing
- Adverse Event Reporting
- MedDRA Coding
- Case Identification
- Case Data Entry
- Regulatory Compliance
- Medical Terminology
- Attention to Detail
- Communication Skills
- Team Collaboration
- Time Management
Work Environment
Selected candidates can expect:
- Individual contributor role.
- Structured onboarding and training.
- Guidance from experienced supervisors.
- Exposure to global pharmaceutical projects.
- Opportunity to work in rotational shifts.
- Career growth within Accenture Life Sciences.
Why Join Accenture?
Working at Accenture offers several advantages:
- Global healthcare projects
- International client exposure
- Strong learning environment
- Career advancement opportunities
- Modern digital work ecosystem
- Industry-leading pharmacovigilance processes
- Professional development programs
- Inclusive and diverse workplace
Who Should Apply?
This role is ideal for professionals who have:
- B.Pharm or M.Pharm qualification
- 1โ3 years of pharmacovigilance experience
- Knowledge of drug safety and ICSR workflows
- Experience with MedDRA coding
- Interest in global pharmacovigilance operations
- Strong analytical and documentation skills
How to Apply
