PHARMAFull-time
Pharmacovigilance Services Associate
CHENNAI (IN)ONSITEPOSTED: 7/1/2026
PHARMAFull-time
HIRING ORGANIZATIONACCENTUREProfessional Services / Management Consulting / Technology Consulting
ROLE DEFINITION & RESPONSIBILITIES
Selected candidates will be responsible for
Performing end-to-end ICSR case processing.
Processing Adverse Events (AE), Serious Adverse Events (SAE), and SUSAR cases.
Reviewing incoming safety reports and validating Individual Case Safety Reports (ICSRs).
Creating and updating cases in Global Safety Databases.
Conducting duplicate checks and data quality review.
Coding adverse events using MedDRA.
Drug coding using WHO Drug Dictionary (WHODD).
Writing accurate medical narratives.
Assessing seriousness and causality.
Processing regulatory submissions according to client SOPs.
Monitoring client mailboxes and safety workflows.
Following up for missing safety information.
Supporting audits, inspections, reconciliation, and pharmacovigilance projects.
Ensuring compliance with global regulatory requirements.
REQUIRED VERIFIED SKILLS
Pharmacovigilance
Drug Safety
Medical Terminology
MedDRA
WHO Drug Dictionary
Safety Databases
Medical Writing
COMPENSATION & REWARDS
₹4.8L - 7.5L per annum
Based on current market trends for 1–3 years of Pharmacovigilance experience in Chennai, the estimated CTC ranges between ₹4.8 LPA – ₹7.5 LPA. Actual compensation depends on candidate experience, skills, and interview performance.
ORGANIZATION CONTEXT & CULTURE
Accenture is a global professional services company providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. It partners with clients across various industries to help them improve their performance and create sustainable value for their stakeholders. The company leverages its extensive industry and technology expertise to drive innovation and transformation.
TEAM SIZE: 700,000+ employees
INDUSTRY: Professional Services / Management Consulting / Technology Consulting
EXPECTED CAREER ROADMAP
Employees benefit from global exposure in pharmacovigilance projects, structured learning and career growth, and opportunities to work with leading pharmaceutical companies in a collaborative work environment.
APPLICATION ADVISORY
Highlight your understanding of drug safety surveillance, adverse event processing, and your ability to work within pharmacovigilance services. Ensure your CV reflects proficiency in medical terminology and regulatory reporting guidelines.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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