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Are you ready to kick-start your career in Pharmacovigilance and Drug Safety? Accenture, a global leader in digital and professional services, is offering a great opportunity for fresh graduates to join their Life Sciences R&D Operations as a Pharmacovigilance Services New Associate.
This full-time role is perfect for those who are passionate about patient safety, regulatory compliance, and the pharmaceutical sector.
Job Details
Position: Pharmacovigilance Services New Associate
Location: Chennai, India
Job Reference: AIOC-S01610262
Experience: 0–1 years (Freshers encouraged to apply)
Qualification Required:
About Accenture
Accenture is a world-renowned professional services organization with expertise in cloud, digital, security, consulting, operations, and Accenture Song. With more than 699,000 employees across 120+ countries, Accenture works with the top global biopharma companies to improve patient outcomes and deliver smarter healthcare solutions.
Role Overview – What Will You Do?
As part of Accenture’s Pharmacovigilance & Drug Safety Surveillance team, you will:
- Handle case intake, identification, and data entry
- Perform MedDRA coding for adverse event reports
- Process ICSRs accurately within timelines
- Execute follow-ups and report submissions as per global regulatory norms
- Manage affiliate mailbox and conduct reconciliation tasks
- Maintain high-quality compliance and documentation standards
You will be working closely with your internal team and supervisor to ensure safe and efficient delivery of PV services.
Skills Required
✔ Detail-oriented with strong analytical ability
✔ Ability to work under pressure and adapt to shifting priorities
✔ Good communication and problem-solving skills
✔ Team collaboration and client service mindset
✔ Willingness to work in rotational shifts
Why This Opportunity Matters?
Joining Accenture as a PV New Associate means:
- A strong beginning in the Pharmacovigilance field
- Exposure to industry-standard drug safety systems
- Career growth into advanced PV and regulatory roles
- Opportunity to work with leading pharmaceutical companies worldwide
Take the first step toward a successful career in Drug Safety!
📌 Apply Now — Don’t miss this opportunity to step into the pharma corporate world with Accenture.
OR
Pharmacovigilance Interview FAQs for Freshers
1️⃣ What is Pharmacovigilance?
Pharmacovigilance (PV) refers to the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any drug-related problem throughout a product’s lifecycle.
2️⃣ What is an Adverse Drug Reaction (ADR)?
An ADR is a harmful or unintended response to a medication that occurs at normal therapeutic doses during proper use.
3️⃣ What is an Adverse Event (AE)?
An AE is any unfavorable medical occurrence after using a medicinal product, not necessarily caused by the drug.
Difference: All ADRs are AEs, but not all AEs are ADRs.
4️⃣ What are the main types of ADRs?
- Serious (life-threatening, hospitalization, disability, death)
- Non-Serious (minor symptoms, no major medical intervention)
5️⃣ What is an ICSR?
ICSR means Individual Case Safety Report, which contains detailed safety information about one patient, one case of an adverse event.
6️⃣ What is MedDRA?
MedDRA stands for Medical Dictionary for Regulatory Activities — a standardized medical terminology used in PV for coding adverse events.
7️⃣ What are the core activities in Pharmacovigilance?
✅ Case intake
✅ Case processing
✅ MedDRA coding
✅ Narrative writing
✅ Follow-ups
✅ Safety reporting to regulatory authorities
8️⃣ What is meant by Serious vs. Non-Serious Case Processing?
- Serious cases need expedited reporting to regulatory bodies (e.g., within 7 or 15 days)
- Non-serious cases follow regular reporting timelines
9️⃣ What is Signal Detection?
It’s the identification of new safety information (unexpected adverse effects) from various data sources to assess drug risk.
🔟 What skills are required for a PV Associate?
- Good medical/clinical knowledge
- Attention to detail
- Strong written communication
- Time management
- Quality and compliance focus
- Knowledge of safety databases (bonus for freshers)
1️⃣1️⃣ Why do you want to build a career in Pharmacovigilance?
A safe answer:
“PV allows me to contribute to patient safety by ensuring medicines are used safely worldwide. It combines my scientific knowledge with analytical and regulatory skills, making it a strong career path for me.”
1️⃣2️⃣ Are you comfortable with rotational shifts?
A professional response:
“Yes, I understand that PV ensures 24/7 patient safety, so I am comfortable working in rotational shifts.”
Bonus Quick Tips for Freshers
- Review basics of clinical trials phases
- Know common regulatory agencies: FDA, EMA, CDSCO
- Practice medical terminology
- Be confident with communication skills
- Show your interest in learning and quality
