Pharmacovigilance Services New Associate (Junior Drug Safety Associate)
Location: Bengaluru, India
Job Type: Full-Time
Experience Required: 0–2 Years
Job Reference: AIOC-S01628146
Function: Pharmacovigilance Operations – Drug Safety Surveillance
Company: Accenture
Job Overview
Accenture is seeking a Pharmacovigilance Services New Associate to join its Life Sciences R&D division in Bengaluru. This entry-level drug safety role is designed for pharmacy and life sciences graduates who are looking to begin or advance their career in pharmacovigilance, adverse event reporting, and global regulatory compliance.
The selected candidate will support pharmacovigilance operations for global biopharmaceutical clients, ensuring accurate processing of safety data and compliance with international drug safety standards.
Experience Required
0 to 2 years of experience in pharmacovigilance, drug safety, clinical research, or related life sciences roles
Fresh graduates with relevant academic exposure to pharmacovigilance and regulatory affairs are encouraged to apply
Basic knowledge of ICSR processing, MedDRA coding, and safety databases is preferred
Educational Qualifications
MSc in Life Sciences or related discipline
Bachelor of Pharmacy (B.Pharm)
Master of Pharmacy (M.Pharm)
Key Responsibilities
Perform case identification and data entry for Individual Case Safety Reports (ICSRs)
Conduct MedDRA coding and ensure accurate safety database documentation
Process, review, and submit adverse event cases in accordance with client and global regulatory requirements
Manage follow-ups and case lifecycle activities as per pharmacovigilance guidelines
Support drug safety surveillance activities across clinical and post-marketing environments
Ensure compliance with international pharmacovigilance regulations and standard operating procedures
Maintain high levels of data accuracy, quality, and documentation integrity
Role Expectations
Handle routine pharmacovigilance and drug safety tasks under supervision
Follow established precedents and general operational guidelines
Work collaboratively within a defined team structure
Operate as an individual contributor within a clearly defined scope of responsibilities
Be flexible to work in rotational shifts as required by project or client demands
Core Skills and Competencies
Foundational understanding of pharmacovigilance operations and adverse event reporting
Knowledge of global drug safety regulations and compliance standards
Strong analytical and data management skills
High attention to detail and process adherence
Effective communication and teamwork capabilities
About Accenture – Life Sciences R&D
Accenture is a global professional services organization with expertise in digital transformation, cloud, security, and operational excellence. Within its Life Sciences R&D vertical, Accenture partners with leading pharmaceutical and biotechnology companies to support clinical development, regulatory services, pharmacovigilance, and patient-centric solutions.
With operations across more than 120 countries, Accenture enables life sciences companies to accelerate innovation while ensuring regulatory compliance and patient safety.
Why Apply for This Pharmacovigilance Role?
Entry-level opportunity in drug safety and pharmacovigilance operations
Exposure to global biopharma clients and international regulatory frameworks
Structured career progression in pharmacovigilance, regulatory affairs, and clinical safety
Opportunity to build expertise in ICSR management, MedDRA coding, and safety database systems
This Pharmacovigilance Services New Associate position in Bengaluru is ideal for pharmacy and life sciences graduates seeking to establish a long-term career in drug safety surveillance, adverse event management, and global regulatory compliance.
Apply through The Pharma Daily to explore pharmacovigilance jobs in India and advance your career in the global pharmaceutical and life sciences industry.
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