Location: Bengaluru, India
Company: Accenture
Job ID: AIOC-S01628146
Job Type: Full-Time
Experience Required: 0–2 Years (Freshers Eligible)
About the Company
Accenture is a leading global professional services organization specializing in digital, cloud, and security solutions. With operations in over 120 countries and a workforce of more than 700,000 professionals, Accenture delivers cutting-edge services across Strategy, Consulting, Technology, and Operations. Within Life Sciences, the organization plays a pivotal role in enabling pharmaceutical and biotechnology companies to accelerate innovation, ensure patient safety, and meet global regulatory standards.
Job Overview
This entry-level Pharmacovigilance role is part of Accenture’s Life Sciences R&D division, focusing on drug safety and risk management. The position is ideal for freshers and early-career professionals looking to build a strong foundation in Pharmacovigilance Operations, including Individual Case Safety Report (ICSR) processing and safety data management.
Key Responsibilities
Perform case identification, data entry, and processing of Individual Case Safety Reports (ICSRs)
Conduct MedDRA coding and ensure accurate safety database entry
Manage case workflows including follow-ups, submissions, and lifecycle tracking
Monitor adverse drug reactions (ADRs) and support signal detection activities
Ensure compliance with global pharmacovigilance regulations and client-specific guidelines
Collaborate with internal teams for quality review and case closure
Maintain data accuracy, completeness, and regulatory timelines in safety reporting
Support routine pharmacovigilance operations under supervision
Required Qualifications
MSc (Life Sciences) / Bachelor of Pharmacy / Master of Pharmacy
Strong understanding or academic exposure to Pharmacovigilance and Drug Safety
Basic knowledge of MedDRA coding and ICSR lifecycle preferred
Good analytical skills and attention to detail
Effective communication and teamwork abilities
Desired Skills and Competencies
Understanding of Pharmacovigilance Operations and regulatory frameworks
Familiarity with clinical research and drug safety processes
Ability to work in a structured, process-driven environment
Willingness to work in rotational shifts as per business requirements
Work Environment and Role Scope
Entry-level individual contributor role with defined responsibilities
Tasks are guided by standard operating procedures and supervision
Opportunity to gain hands-on experience in global pharmacovigilance projects
Exposure to real-world drug safety case processing and regulatory workflows
Why This Role is Important for Your Career
This position serves as a gateway into the Pharmacovigilance and Drug Safety domain. It provides foundational experience in ICSR processing, regulatory compliance, and safety data handling, making it an ideal starting point for careers such as Drug Safety Associate, Medical Reviewer, or Pharmacovigilance Specialist.
Equal Employment Opportunity Statement
Accenture is committed to creating an inclusive workplace. All employment decisions are based on merit, qualifications, and business needs, without discrimination based on race, gender, age, disability, religion, sexual orientation, or any other protected status.
How to Apply
Candidates can apply through official company channels. For more verified Pharmacovigilance jobs for freshers and experienced professionals, visit ThePharmaDaily.com and explore global opportunities in Drug Safety, Clinical Research, and Regulatory Affairs.
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