Accenture Hiring for Pharmacovigilance Services Associate (0–2 Years) | Bengaluru | Apply Now
Are you looking to launch your career in the pharmaceutical and life sciences domain? This is an excellent opportunity for fresh graduates and early professionals to join one of the world’s leading consulting and technology companies. Accenture is hiring for the role of Pharmacovigilance Services Associate at its Bengaluru location.
If you have a passion for drug safety, clinical research, or pharmacovigilance, and want to work with a global leader in life sciences operations, this job is tailor-made for you.
About Accenture
Accenture is a global professional services company known for its capabilities in digital, cloud, and security solutions. With over 699,000 employees across 120+ countries, Accenture combines technology and human ingenuity to deliver innovation across industries.
The company operates through several verticals, including:
Strategy & Consulting
Technology & Operations Services
Accenture Song (customer experience and marketing innovation)
Accenture’s Life Sciences R&D vertical partners with the world’s leading biopharma and healthcare companies to enhance patient outcomes, streamline regulatory compliance, and ensure drug safety through advanced data-driven operations.
Visit: 🌐 www.accenture.com
Job Overview
Role: Pharmacovigilance Services Associate
Job No.: AIOC-S01589024
Employment Type: Full-Time
Experience: 0 – 2 Years (Freshers Welcome)
Location: Bengaluru, India
Qualification: Any Graduation
Language Requirement: Japanese (Elementary – JLPT N3 to N5 Level)
Industry: Life Sciences / Pharmaceuticals / Healthcare Operations
About the Role
The Pharmacovigilance Services Associate will be aligned with Accenture’s Life Sciences R&D vertical under the Clinical, Pharmacovigilance & Regulatory division. This team plays a key role in drug safety surveillance, regulatory compliance, and pharmacovigilance operations, ensuring the safety and efficacy of pharmaceuticals across global markets.
Your primary responsibility will be to support pharmacovigilance and drug safety operations by managing case processing, safety data entry, medical coding, and report submissions in accordance with global regulatory requirements.
Key Responsibilities
As a Pharmacovigilance Services Associate, your day-to-day tasks will include:
Case Processing and Data Entry
Perform accurate data entry of Individual Case Safety Reports (ICSRs).
Ensure all required data fields are completed according to client SOPs and global regulatory guidelines.
MedDRA Coding and Classification
Apply correct MedDRA codes for reported adverse events and reactions.
Ensure consistent terminology and alignment with international coding standards.
Report Management
Manage affiliate mailboxes for receipt of case information.
Perform reconciliation of reports and track follow-ups for both serious and non-serious cases.
Regulatory Compliance
Maintain compliance with global pharmacovigilance regulations (FDA, EMA, MHRA).
Adhere to Good Pharmacovigilance Practices (GVP) and internal quality standards.
Collaboration and Documentation
Collaborate with team members to ensure timely submission of safety reports.
Maintain documentation and audit readiness for client and internal reviews.
Required Skills and Competencies
To succeed in this role, candidates should demonstrate the following skills and attributes:
Agility for quick learning and adaptability to new processes.
Attention to detail and commitment to quality in data entry and documentation.
Teamwork and effective communication skills.
Language Ability: Basic proficiency in Japanese (JLPT N3–N5) is required.
Technical Skills: Familiarity with safety databases (e.g., Argus, ARISg) is a plus.
Educational Qualification
Any Graduation – preferably in Life Sciences, Pharmacy, Nursing, Microbiology, or Biotechnology.
Candidates from non-life sciences backgrounds may also apply if they possess strong analytical skills and interest in pharmacovigilance.
Experience Required
0 to 2 Years of experience in Pharmacovigilance, Drug Safety, or Clinical Data Management.
Fresh graduates with a strong foundation in healthcare or life sciences are encouraged to apply.
Work Environment and Culture
Work Location: Bengaluru (Work from Office).
Team Structure: Collaborative team environment with moderate supervision.
Work Shift: Rotational shifts (may include night shifts based on project requirements).
You will primarily interact with peers within Accenture, and your contributions will directly impact your team’s performance and client satisfaction.
Why Join Accenture’s Pharmacovigilance Team?
1. Global Exposure
Work on international pharmacovigilance projects supporting leading pharmaceutical and biotech companies worldwide.
2. Continuous Learning
Access Accenture’s Life Sciences training modules and digital upskilling programs, helping you enhance both technical and professional skills.
3. Cutting-Edge Technology
Use industry-standard tools and platforms for safety data management, AI-assisted surveillance, and automated regulatory reporting.
4. Diversity and Inclusion
Accenture is an Equal Opportunity Employer, fostering a workplace that values diversity, inclusion, and equality for all employees.
5. Career Growth
Begin your career with structured learning paths and performance-based progression opportunities in Pharmacovigilance Operations, Clinical Research, or Regulatory Affairs.
Equal Employment Opportunity Statement
Accenture is committed to creating an inclusive work environment.
All employment decisions are made without regard to:
Age, race, color, religion, sex, nationality, ancestry, disability, veteran status, or sexual orientation.
Gender identity, genetic information, marital status, or citizenship.
Accenture ensures equal access to opportunities for all individuals.
How to Apply
Interested candidates can apply directly through Accenture’s career portal or visit the job listing page using the job ID provided below.
🔹 Job ID: AIOC-S01589024
🔹 Role: Pharmacovigilance Services Associate
🔹 Location: Bengaluru
🔹 Experience: 0–2 Years
🔹 Language: Japanese (Elementary, JLPT N3–N5)
Application Steps:
Search for the job using Job ID: AIOC-S01589024
Submit your resume and complete the online assessment if prompted.
Shortlisted candidates will be contacted for interviews and language proficiency evaluation.
Interview Tips
✅ Prepare for Basic Pharmacovigilance Concepts:
Understand case processing flow, ICSR structure, and regulatory timelines (15-day / 30-day reporting rules).
✅ Highlight Japanese Language Skills:
Since the role involves basic Japanese communication, emphasize your JLPT certification or equivalent proficiency.
✅ Demonstrate Attention to Detail:
Accuracy in data entry and MedDRA coding is crucial for pharmacovigilance roles.
✅ Be Ready for Scenario-Based Questions:
Expect practical questions like “How would you handle a serious adverse event report?”
Conclusion
The Accenture Pharmacovigilance Services Associate role is a great opportunity for freshers and early-career professionals looking to enter the fast-growing field of drug safety and regulatory compliance.
With the chance to work in a global environment, develop specialized pharmacovigilance skills, and contribute to improving patient safety worldwide, this position offers a rewarding start to your career in the life sciences industry.
If you’re passionate about healthcare, technology, and safety — apply today and join Accenture’s mission to bring innovation and safety excellence to the global pharmaceutical ecosystem.
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