Pharmacovigilance Services Associate / Sr Analyst
Accenture is hiring Pharmacovigilance Services Associates and Pharmacovigilance Services Sr Analysts for its Life Sciences R&D division in Bengaluru. This opportunity is ideal for Pharmacy professionals with experience in Pharmacovigilance Operations, Drug Safety Surveillance, ICSR Processing, Adverse Event Reporting, and MedDRA Coding.
Selected candidates will support global pharmacovigilance operations, safety case processing, regulatory compliance, safety database activities, and adverse event management for leading pharmaceutical and biotechnology clients.
Professionals seeking career growth in Drug Safety, Pharmacovigilance Operations, Regulatory Affairs, and Global Safety Surveillance should explore this opportunity.
📋 Job Overview
| Particulars | Details |
|---|---|
| Company | Accenture |
| Position | PV Services Associate / Sr Analyst |
| Location | Bengaluru, Karnataka |
| Department | Life Sciences R&D |
| Work Mode | Onsite / Hybrid (Business Requirement) |
| Experience | 1–3 Years (Associate), 4–8 Years (Sr Analyst) |
| Qualification | B.Pharm / M.Pharm |
| Application Mode | Online Application |
💼 Key Responsibilities
- Perform Individual Case Safety Report (ICSR) processing.
- Handle adverse event case identification and data entry.
- Conduct MedDRA coding activities.
- Manage safety database operations and documentation.
- Support adverse event follow-up and case submissions.
- Ensure compliance with global pharmacovigilance regulations.
- Review and evaluate drug safety information.
- Maintain regulatory documentation and reporting standards.
- Collaborate with internal teams to resolve case processing issues.
- Support drug safety surveillance activities.
🎓 Eligibility Criteria
Educational Qualifications
- B.Pharm
- M.Pharm
Experience Requirements
- 1–3 Years for Pharmacovigilance Services Associate
- 4–8 Years for Pharmacovigilance Services Sr Analyst
- Experience in ICSR Processing
- Drug Safety Surveillance Experience
- MedDRA Coding Knowledge
- Safety Database Experience Preferred
🧠 Required Skills
- Pharmacovigilance Operations
- Drug Safety Surveillance
- ICSR Processing
- Adverse Event Reporting
- MedDRA Coding
- Safety Database Management
- Regulatory Compliance
- Case Processing
- Documentation Skills
- Attention to Detail
- Communication Skills
- Analytical Thinking
Top 100 Pharmacovigilance Interview Questions
Pharmacovigilance Quiz
Drug Safety Analyst Quiz
💰 Salary & Benefits
Based on current Pharmacovigilance industry benchmarks:
Pharmacovigilance Services Associate: ₹4.5 LPA – ₹8 LPA
Pharmacovigilance Services Sr Analyst: ₹8 LPA – ₹14 LPA
Actual compensation may vary based on experience, MedDRA expertise, safety database knowledge, and interview performance.
Employee Benefits
- Global Pharmaceutical Project Exposure
- Career Growth in Life Sciences R&D
- Learning & Development Programs
- Industry Certifications & Training
- Collaborative Work Environment
- Health & Wellness Benefits
- Professional Development Opportunities
- International Client Exposure
🌟 Why Join Accenture?
- Work with Leading Global Pharma & Biotech Clients
- Exposure to End-to-End Pharmacovigilance Operations
- Strong Learning & Upskilling Programs
- Opportunity to Work on Global Safety Databases
- Career Growth in Drug Safety & Regulatory Functions
- Technology-Driven Healthcare Environment
- Global Career Mobility Opportunities
- Industry-Leading Work Culture
📈 Career Growth Opportunities
Professionals can advance into several specialized Drug Safety and Regulatory roles:
- Drug Safety Associate
- Senior Drug Safety Associate
- Pharmacovigilance Specialist
- Aggregate Reporting Associate
- Safety Scientist
- Risk Management Specialist
- Pharmacovigilance Team Lead
- Global Safety Manager
Top 100 Pharmacovigilance Interview Questions
Pharmacovigilance Quiz
Drug Safety Analyst Quiz
Pharmacovigilance Salary Guide
📑 Resume Tips for Pharmacovigilance Professionals
- Highlight ICSR Processing Experience.
- Mention MedDRA Coding Expertise.
- Include Safety Database Knowledge.
- Showcase Adverse Event Reporting Activities.
- Mention Regulatory Compliance Experience.
- Keep Resume ATS-Friendly and Achievement Focused.
📌 How to Apply?
Before applying, ensure your resume highlights Pharmacovigilance Operations experience, ICSR processing, MedDRA coding, Drug Safety Surveillance activities, and safety database expertise.
Read our complete Healthcare & Pharma Job Application Guide:
Healthcare & Pharma Job Application Guide🚀 Apply Now – Pharmacovigilance Services Associate
Apply for Pharmacovigilance Services Associate🚀 Apply Now – Pharmacovigilance Services Sr Analyst
Apply for Pharmacovigilance Services Sr Analyst📚 Related Resources from HiTechPlus
❓ Frequently Asked Questions
Q. Which qualifications are eligible?
B.Pharm and M.Pharm candidates can apply.
Q. What experience is required?
1–3 years for Associate and 4–8 years for Sr Analyst roles.
Q. Is MedDRA coding experience required?
Yes, MedDRA coding knowledge is highly preferred.
Q. What location is this role based in?
Bengaluru, Karnataka.
Q. What domain will candidates work in?
Pharmacovigilance Operations, Drug Safety Surveillance, ICSR Processing, and Regulatory Compliance.
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