Pharmacovigilance Services Associate – Drug Safety Operations
Location: Bengaluru, India
Employment Type: Full-Time
Experience Required: 0–2 Years (Freshers & Early Professionals)
Job ID: AIOC-S01622134
Industry: Pharmacovigilance | Drug Safety | Life Sciences
Qualification: B.Pharm / M.Pharm
About the Company
Accenture is a global professional services leader with strong capabilities across digital, cloud, and security. With a workforce of over 784,000 professionals serving clients in more than 120 countries, Accenture combines deep industry expertise with advanced technology to deliver measurable outcomes.
Within Accenture’s Life Sciences R&D vertical, teams support the full spectrum of pharmaceutical and biotech operations, including clinical research, regulatory affairs, pharmacovigilance, and patient safety services—helping global biopharma organizations improve patient outcomes and regulatory compliance.
Job Overview
The Pharmacovigilance Services Associate will be part of Accenture’s Pharmacovigilance & Drug Safety Operations team. This role is ideal for freshers or professionals with up to 2 years of experience who are looking to build a career in drug safety, ICSR processing, and global pharmacovigilance operations.
The position focuses on case processing, safety data management, MedDRA coding, and regulatory submissions in compliance with global pharmacovigilance regulations.
Key Responsibilities
Perform end-to-end ICSR case processing, including case intake, data entry, triage, and follow-ups
Conduct MedDRA coding for adverse events, medical history, and concomitant medications
Ensure accurate and timely case submissions as per global regulatory requirements and client guidelines
Manage safety data within validated safety databases
Support case identification, narrative writing, and quality checks
Follow standard operating procedures (SOPs), work instructions, and regulatory guidelines
Resolve routine operational issues by referring to established guidelines and processes
Collaborate closely with team members and report to the immediate supervisor
Work as an individual contributor within a structured pharmacovigilance operations team
Adapt to rotational shift schedules based on business requirements
Required Qualifications & Experience
Education:
Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm)
Experience:
0–2 years of experience in Pharmacovigilance or Drug Safety Operations
Freshers with relevant academic exposure or training in pharmacovigilance are encouraged to apply
Skills & Competencies
Basic understanding of Pharmacovigilance and Drug Safety Surveillance
Knowledge of ICSR processing, MedDRA coding, and safety case workflows
Familiarity with global regulatory requirements (ICH, GVP) is an advantage
Strong attention to detail and accuracy
Ability to follow structured processes and guidelines
Good communication and teamwork skills
Willingness to learn and adapt in a regulated environment
Why Join Accenture
Opportunity to work with global pharmaceutical and biotech clients
Structured learning and career development in pharmacovigilance
Exposure to global safety databases and regulatory standards
Strong mentorship and team-based work culture
A platform to build a long-term career in drug safety and life sciences
Equal Opportunity Statement
Accenture is an equal opportunity employer. All employment decisions are made without regard to race, religion, gender, age, disability, or any other legally protected status. Candidates with transferable skills and relevant academic backgrounds are encouraged to apply.
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