Accenture Hiring Pharmacovigilance Services New Associate – Drug Safety & PV Operations Role
Accenture is hiring Pharmacovigilance Services New Associate for its Life Sciences R&D division in Chennai.
This opportunity is ideal for candidates from B.Pharm and Life Sciences backgrounds who want to build careers in Pharmacovigilance, Drug Safety Operations, ICSR Processing, MedDRA Coding, and Clinical Safety Services.
📋 Job Overview
- Company: Accenture
- Location: Chennai, India
- Role: Pharmacovigilance Services New Associate
- Department: Life Sciences R&D
- Category: Pharmacovigilance & Drug Safety
- Qualification: Bachelor of Pharmacy / Bachelor Degree in Life Sciences
- Experience Required: 0–1 Years
- Shift: Rotational Shifts may apply
📌 Key Responsibilities
- Create and manage case identification activities
- Perform ICSR case processing and follow-ups
- Support data entry and MedDRA coding activities
- Maintain safety database records as per guidelines
- Ensure compliance with global regulatory requirements
- Support adverse event monitoring and reporting
- Work with Pharmacovigilance & Drug Safety teams
- Handle routine safety operations tasks under supervision
- Maintain documentation accuracy and quality standards
- Support patient safety and risk management activities
🎓 Eligibility Criteria
- Bachelor of Pharmacy (B.Pharm)
- Bachelor Degree in Life Sciences
- Good communication and analytical skills
- Understanding of Pharmacovigilance concepts preferred
- Knowledge of adverse event reporting beneficial
- Attention to detail and documentation accuracy
- Ability to work in rotational shifts
- Team collaboration and MS Office skills preferred
⭐ Preferred Skills
- ICSR Processing
- MedDRA Coding
- Drug Safety Operations
- Adverse Event Reporting
- Safety Database Management
- Regulatory Compliance
🌍 Why Join Accenture?
- Opportunity to work with global biopharma clients
- Strong career growth in Pharmacovigilance & Drug Safety
- Exposure to international healthcare projects
- Hands-on learning in Life Sciences R&D operations
- Professional training and skill development opportunities
- Collaborative and inclusive work culture
📄 Resume Tips
- Highlight Pharmacovigilance knowledge and certifications
- Mention Drug Safety internships or academic projects
- Add MedDRA, ICSR, or AE reporting exposure if available
- Use ATS-friendly resume formatting
- Showcase communication and analytical skills
- Mention MS Office and documentation skills clearly
- Keep resume concise, clean, and professional
🎯 Interview Tips for Pharmacovigilance Associate Role
- Prepare Pharmacovigilance and Drug Safety basics thoroughly
- Understand ICSR, MedDRA Coding, and adverse event concepts
- Revise serious vs non-serious adverse event differences
- Practice questions related to AE case processing workflows
- Be ready to explain internships, certifications, or projects
- Prepare examples showcasing teamwork and communication skills
- Research Accenture Life Sciences division before interview
- Maintain professional communication during interview rounds
❓ Frequently Asked Questions (FAQs)
1. Who can apply for this role?
Candidates with B.Pharm or Life Sciences background can apply for this role.
2. Is this role suitable for freshers?
Yes, candidates with 0–1 years experience can apply.
3. What is MedDRA Coding?
MedDRA Coding is the process of coding adverse events using the Medical Dictionary for Regulatory Activities.
4. What is ICSR in Pharmacovigilance?
ICSR stands for Individual Case Safety Report used in adverse event reporting.
5. Are rotational shifts involved?
Yes, this role may require rotational shifts.
🧩 Fun Learning & Career Growth
Improve your Pharmacovigilance and Drug Safety knowledge with quizzes and learning resources.
🚀 Apply Now
Kindly read the complete job description carefully before applying. Make sure your qualifications, skills, and Pharmacovigilance knowledge align with the role requirements.
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