Accenture Hiring Pharmacovigilance Services Associate - Bengaluru
Are you seeking high-paying Accenture Pharmacovigilance Jobs or Drug Safety Careers in Bengaluru? Leading global professional services firm Accenture has announced recruitment for a Pharmacovigilance Services Associate. This full-time position is based at its Bengaluru facility and is open to graduates with 0 to 3 years of experience.
This role offers an exceptional opportunity to support global biopharmaceutical companies in pharmacovigilance, ICSR data entry, and medical coding. To prepare your registration details effectively, check out our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | Pharmacovigilance Services Associate |
| Company | Accenture |
| Location | Bengaluru, Karnataka, India |
| Employment Type | Full-Time |
| Shift | Rotational Shifts |
| Experience Required | 0 - 3 Years (Freshers & Experienced) |
| Qualifications | B.Pharm, M.Pharm |
| Application Deadline | Apply Immediately (Not Mentioned) |
| Job ID | AIOC-S01652148-1 |
💼 Key Responsibilities
1. Case Processing Activities
- Perform case identification and intake of incoming adverse event reports.
- Conduct accurate data entry of patient details and events into safety databases.
- Process Individual Case Safety Reports (ICSRs) in compliance with global timelines.
- Ensure complete adherence to global pharmacovigilance and drug safety regulations.
2. MedDRA Coding
- Perform medical coding of adverse events, medical histories, and medications using MedDRA terminology.
- Review and validate coded medical information to ensure coding accuracy and consistency.
3. Drug Safety Surveillance
- Monitor adverse events and safety data across assigned client programs.
- Support pharmacovigilance operational tasks and assist in safety evaluations.
4. Regulatory Compliance & Quality
- Prepare and submit safety reports according to standard operating procedures (SOPs) and client agreements.
- Manage case follow-up documentation and perform data reconciliation.
- Support quality review processes and ensure audit readiness at all times.
Adverse event processing and coding require a clear understanding of drug safety rules. Test your technical knowledge with our guide of the Top 100 Entry Level Pharmacovigilance Questions.
🎓 Eligibility Criteria
Candidates possessing the following qualifications are eligible to apply:
- Degrees: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).
- Experience: 0 to 3 years of pharmacovigilance experience. Freshers with strong training or interns are also eligible to apply.
- Prior working knowledge of safety databases (e.g. Argus) and ICSR workflows is highly preferred for experienced candidates.
For pharmacy graduates planning their career and comparing national vs global salary growth, check our guide on B.Pharm Career: India vs USA.
Required Core Skills
- Expertise in Pharmacovigilance Operations and Drug Safety Surveillance.
- Proficiency in MedDRA terminology coding and ICSR processing rules.
- Strong attention to detail with high analytical and critical thinking capabilities.
- Exceptional communication skills (both written and verbal) in English.
- Ability to work in rotational shifts and manage time under strict client timelines.
💰 Salary & Employee Benefits
- Competitive base salary matching industry standards for entry-level and experienced PV professionals.
- Comprehensive medical insurance and employee wellness benefits.
- Access to global learning, structured professional training, and certification programs.
- Opportunity to work with global biopharmaceutical companies.
- Diverse and inclusive workplace culture encouraging long-term career growth.
To see how drug safety salaries scale between India and international regions, read our analysis on Pharmacovigilance Salary: India vs USA.
🌟 Why Join Accenture?
- Accenture is a leading multinational professional services firm serving clients in over 120 countries.
- Excellent environment to build skills in safety systems, cloud-based data management, and GVP (Good Pharmacovigilance Practices) guidelines.
- Strong stepping stone to transition into senior case processor, quality reviewer, or safety lead roles.
📑 Resume Tips for Accenture
- Clearly highlight your B.Pharm or M.Pharm degree and any pharmacovigilance certifications.
- Detail your experience or training in ICSR processing, MedDRA coding, and Argus database.
- Keep your resume clean, professional, and optimized for ATS systems.
🎯 Accenture Pharmacovigilance Associate Interview Questions
- What are the four minimum criteria required for a valid adverse event case?
- What is MedDRA and explain its hierarchy from LLT to SOC.
- How do you distinguish between serious and non-serious adverse events?
- What is the difference between an adverse event (AE) and an adverse drug reaction (ADR)?
- How do you handle pressure and maintain data accuracy during high-volume case processing?
📌 How to Apply?
Interested and eligible candidates can submit their applications online directly through Accenture's official Workday portal using the link below. Since no specific application deadline is mentioned, candidates are advised to apply immediately. For help setting up your Workday application profile, read our guide on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. What is the application deadline?
No deadline is mentioned in the official post. Candidates are advised to apply immediately.
Q. Who is eligible to apply?
B.Pharm and M.Pharm graduates.
Q. What is the required experience?
0 to 3 years of experience in pharmacovigilance operations.
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