Accenture has announced multiple Pharmacovigilance Services Associate jobs in Bengaluru for candidates interested in pharmacovigilance, drug safety and ICSR case processing. Five separate Pharmacovigilance Services Associate requisitions have been listed, creating an excellent opportunity for candidates with relevant drug safety experience.
The Accenture Pharmacovigilance Associate jobs 2026 involve Individual Case Safety Report (ICSR) processing, case identification, safety data entry, MedDRA coding, follow-up activities, reconciliation and regulatory submission activities.
Candidates with 1–3 years of experience are specified for these positions. Qualification requirements vary by individual requisition: one provided listing specifies B.Pharm/M.Pharm, while another specifies Any Graduation.
Accenture Pharmacovigilance Job Overview
| Particular | Details |
|---|---|
| Company | Accenture |
| Designation | Pharmacovigilance Services Associate |
| Skill | Pharmacovigilance & Drug Safety Surveillance |
| Location | Bengaluru |
| Employment | Full-Time |
| Experience | 1–3 Years |
| Qualification | B.Pharm / M.Pharm / Any Graduation depending on requisition |
| Number of Associate Requisitions | 5 |
| Work Schedule | Rotational shifts may be required |
| Job IDs | AIOC-S01661196, AIOC-S01661197, AIOC-S01661198, AIOC-S01661199, AIOC-S01661200 |
What Will You Do?
As a Pharmacovigilance Services Associate at Accenture, you will work as part of the drug safety operations team and support the processing and management of safety reports.
The position primarily focuses on Individual Case Safety Reports and associated pharmacovigilance operational activities.
Key Responsibilities
- Manage the affiliate pharmacovigilance mailbox.
- Perform reconciliation of safety reports according to established processes.
- Perform written follow-up attempts for both serious and non-serious cases.
- Support identification and creation of Individual Case Safety Reports (ICSRs).
- Perform accurate safety case data entry.
- Conduct MedDRA coding of reported adverse events and relevant medical information.
- Process pharmacovigilance cases according to client guidelines.
- Support submission of safety cases according to applicable global regulatory requirements.
- Perform follow-up activities for incomplete or additional safety information.
- Maintain accurate pharmacovigilance documentation.
- Follow established SOPs, procedures and general guidelines.
- Resolve routine operational problems using established precedents and procedures.
- Coordinate with team members and the direct supervisor.
- Complete assigned work within the predetermined scope and quality requirements.
Qualifications
Accenture has listed different educational requirements across the Pharmacovigilance Services Associate requisitions.
Relevant qualifications include:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- Any Graduation for requisitions where this eligibility is explicitly specified
Candidates should carefully check the qualification criteria on the respective Accenture application page before applying.
Experience Required
The provided Accenture job descriptions specify:
1–3 years of experience
Candidates with prior experience in pharmacovigilance, drug safety operations or ICSR case processing may be particularly relevant for these positions.
Skills Required for Accenture Pharmacovigilance Jobs
Candidates should have knowledge or practical exposure to areas such as:
- Pharmacovigilance
- Drug Safety Surveillance
- ICSR Processing
- Adverse Event Case Processing
- Case Identification
- Safety Data Entry
- MedDRA Coding
- Serious and Non-Serious Cases
- Case Follow-up
- Affiliate Mailbox Management
- Safety Report Reconciliation
- Regulatory Safety Reporting
- Pharmacovigilance Databases
- Global Drug Safety Requirements
- Pharmacovigilance SOPs and Guidelines
The primary skill specified by Accenture is Pharmacovigilance & Drug Safety Surveillance – P1.
Role and Working Environment
The Pharmacovigilance Services Associate position is an individual contributor role within a defined team structure.
Associates are expected to handle routine problems using established guidelines and precedents. Most interactions will be with members of the immediate team and direct supervisor.
Detailed to moderate instructions may be provided for regular tasks, while new assignments may involve more detailed guidance.
Candidates should also note that rotational shifts may be required depending on business and project requirements.
Why Consider This Pharmacovigilance Opportunity?
This opportunity can provide relevant industry exposure in several core areas of pharmacovigilance operations, including:
- End-to-end ICSR workflow exposure
- Drug safety case processing
- MedDRA coding
- Safety database operations
- Serious and non-serious case handling
- Follow-up management
- Global regulatory reporting processes
- Pharmacovigilance quality and compliance procedures
Working in these areas can strengthen practical experience relevant to broader careers in drug safety and pharmacovigilance operations.
Accenture Pharmacovigilance Job IDs
Five Pharmacovigilance Services Associate requisitions were provided for Bengaluru:
- AIOC-S01661196
- AIOC-S01661197
- AIOC-S01661198
- AIOC-S01661199
- AIOC-S01661200
Applicants should avoid submitting duplicate applications unnecessarily and should review the qualification requirements of each requisition before applying.
How to Apply for Accenture Pharmacovigilance Jobs
Eligible candidates can apply through the official Accenture careers portal.