Job Title: Pharmacovigilance Services New Associate
Location: Bengaluru, India
Job ID: AIOC-S01628166
Employment Type: Full-Time
Experience Required: 0–2 Years
Pharmacovigilance Services New Associate – Entry-Level Drug Safety Role in Bengaluru
A leading global professional services organization, Accenture, is hiring a Pharmacovigilance Services New Associate for its Life Sciences R&D vertical in Bengaluru. This opportunity is ideal for fresh graduates and early-career professionals looking to build a long-term career in pharmacovigilance, drug safety surveillance, and regulatory compliance within the biopharma sector.
About the Company
Accenture is a multinational professional services firm specializing in digital, cloud, and security solutions. Operating in more than 120 countries with over 784,000 professionals globally, the company delivers services across Strategy & Consulting, Technology, Operations, and Accenture Song. Its Life Sciences R&D division supports pharmaceutical and biotechnology organizations across research, clinical trials, regulatory services, pharmacovigilance, and patient-centric solutions.
Role Overview – Pharmacovigilance & Drug Safety Surveillance
The selected candidate will work within the Clinical, Pharmacovigilance & Regulatory division under the Life Sciences vertical. The role focuses on monitoring, assessing, and ensuring the safety of pharmaceutical products in compliance with global regulatory standards.
Pharmacovigilance operations involve the detection, evaluation, documentation, and prevention of adverse drug reactions (ADRs) and other drug-related issues. The objective is to safeguard patient health while maintaining regulatory compliance and data integrity.
Key Responsibilities
Perform case identification and safety data entry into pharmacovigilance databases
Conduct MedDRA coding for adverse event reports
Process and manage Individual Case Safety Reports (ICSRs)
Ensure accurate case processing, submission, and follow-ups
Comply with client guidelines and global pharmacovigilance regulations
Work under detailed supervision and established SOPs
Collaborate with internal teams and direct supervisors
Work in rotational shifts, if required
This is an entry-level individual contributor role where decisions primarily impact assigned tasks and are closely supervised.
Required Qualifications
MSc (Life Sciences)
Bachelor of Pharmacy (B.Pharm)
Master of Pharmacy (M.Pharm)
Experience Required
0–2 years of experience in pharmacovigilance, drug safety, or related life sciences roles
Freshers with relevant academic exposure to pharmacovigilance are encouraged to apply
Ideal Candidate Profile
Strong understanding of pharmacovigilance processes and regulatory frameworks
Basic knowledge of ICSR case processing and MedDRA coding
High attention to detail and accuracy
Ability to follow structured guidelines and compliance standards
Strong communication and teamwork skills
Why Apply for This Pharmacovigilance Role in Bengaluru?
This opportunity provides structured industry exposure in global pharmacovigilance operations, hands-on experience in drug safety case processing, and career growth within a leading multinational organization.
Apply through ThePharmaDaily.com to start your career as a Pharmacovigilance Services New Associate in Bengaluru.
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