Pharmacovigilance Services Associate
Location: Bengaluru, India
Job ID: AIOC-S01625967
Employment Type: Full-Time
Experience Required: 0–2 years (1–3 years preferred)
Category: Pharmacovigilance / Drug Safety / Life Sciences
About the Organization
Accenture is a global professional services leader with expertise in digital, cloud, security, technology, and intelligent operations. With operations in over 120 countries and a workforce of more than 784,000 professionals, Accenture partners with leading life sciences and biopharmaceutical organizations to accelerate innovation and improve patient outcomes.
Within its Life Sciences R&D vertical, Accenture supports pharmaceutical and biotechnology companies across clinical research, regulatory services, pharmacovigilance, and patient safety operations.
Role Overview
The Pharmacovigilance Services Associate will support global drug safety and pharmacovigilance operations, ensuring compliance with regulatory standards and client requirements. The role involves managing Individual Case Safety Reports (ICSRs), adverse event processing, MedDRA coding, and safety database documentation.
This position is ideal for early-career pharmacy graduates seeking hands-on experience in pharmacovigilance, drug safety surveillance, and regulatory compliance within a structured and quality-driven environment.
Key Responsibilities
Pharmacovigilance & Drug Safety Operations
Perform case identification, data entry, and processing of Individual Case Safety Reports (ICSRs)
Conduct MedDRA coding and ensure accurate safety data documentation
Manage case follow-ups and submissions in accordance with global regulatory requirements
Review and validate safety data received from healthcare professionals, patients, and clinical sources
Maintain compliance with client guidelines, internal SOPs, and international pharmacovigilance standards
Data Quality & Compliance
Ensure timely and accurate case processing within established service-level agreements
Support safety database management and documentation updates
Adhere to global pharmacovigilance regulations and Good Pharmacovigilance Practices (GVP)
Participate in quality checks and audits as required
Team Collaboration & Process Adherence
Work under defined guidelines and supervision to resolve routine operational issues
Collaborate within the assigned team and report to the direct supervisor
Follow detailed instructions for new assignments and daily deliverables
Contribute as an individual team member within a defined scope of work
Education & Experience Requirements
Educational Qualifications
Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm)
Professional Experience
0–2 years of experience in pharmacovigilance, drug safety, or related life sciences roles
1–3 years of relevant experience preferred in safety case processing or ICSR management
Required Skills & Competencies
Technical Skills
Basic understanding of pharmacovigilance operations and drug safety surveillance
Familiarity with ICSR processing and MedDRA coding
Knowledge of global pharmacovigilance regulations and compliance standards
Experience working with safety databases is an advantage
Professional Skills
Strong attention to detail and data accuracy
Good written and verbal communication skills
Ability to manage routine tasks within defined timelines
Analytical problem-solving skills within structured guidelines
Ability to work in rotational shifts, if required
Work Environment
Office-based role in Bengaluru, India
May require rotational shifts based on business needs
Structured team-based environment with defined workflows
Why Apply Through ThePharmaDaily?
Access opportunities with leading global life sciences employers
Build foundational experience in pharmacovigilance and drug safety
Gain exposure to international regulatory compliance standards
Advance your career in clinical research and pharmaceutical operations
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