Pharmacovigilance Services Analyst
Job ID: AIOC-S01619394
Company: Accenture
Location: Bengaluru, India
Employment Type: Full-Time
Functional Area: Pharmacovigilance Operations | Drug Safety Surveillance
Experience Required: 3–5 years
Education: B.Pharm / M.Pharm / MSc (Life Sciences or related field)
About Accenture
Accenture is a leading global professional services organization with expertise across digital, cloud, security, and intelligent operations. With a workforce of over 699,000 professionals serving clients in more than 120 countries, Accenture delivers comprehensive solutions through Strategy & Consulting, Technology, Operations, and Accenture Song. Within the Life Sciences R&D vertical, Accenture supports pharmaceutical and biotech organizations across clinical research, regulatory affairs, pharmacovigilance, and patient services.
Role Overview
The Pharmacovigilance Services Analyst will support global drug safety operations as part of Accenture’s Clinical, Pharmacovigilance & Regulatory practice. This role is ideal for professionals with hands-on experience in ICSR processing, MedDRA coding, and safety database management, contributing to patient safety and regulatory compliance across multiple markets.
Key Responsibilities
Perform end-to-end ICSR case processing, including case intake, triage, and accurate data entry.
Conduct MedDRA coding, narrative writing, and case quality checks in accordance with SOPs.
Manage case submissions and follow-ups in global safety databases as per regulatory timelines.
Monitor and evaluate adverse drug reactions (ADRs) from clinical trials, post-marketing sources, and literature.
Ensure compliance with global pharmacovigilance regulations (ICH-GCP, GVP, FDA, EMA).
Analyze and resolve low to moderate complexity pharmacovigilance issues using standard guidelines.
Collaborate with internal teams and supervisors, with limited exposure to clients or senior management.
Contribute as an individual team member within a focused scope of work.
Adapt to rotational shift requirements based on project needs.
Required Skills & Competencies
Strong understanding of Pharmacovigilance Operations and Drug Safety Surveillance.
Practical experience in ICSR processing, MedDRA coding, and safety database workflows.
Familiarity with clinical trial and post-marketing safety reporting processes.
Knowledge of international pharmacovigilance regulations and compliance standards.
Good analytical skills with attention to detail and documentation accuracy.
Ability to work with moderate supervision and follow structured workflows.
Experience & Qualification Criteria
3 to 5 years of relevant experience in pharmacovigilance or drug safety operations.
Educational qualification in Pharmacy or Life Sciences (B.Pharm / M.Pharm / MSc).
Experience working with global clients or multinational pharmacovigilance programs is an advantage.
Why Join Accenture Life Sciences?
This role offers exposure to global safety programs, established pharmacovigilance frameworks, and long-term career growth within a leading life sciences consulting and operations organization. Accenture provides continuous learning, structured progression, and the opportunity to contribute directly to patient safety worldwide.
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