Job Title
Pharmacovigilance Services – New Associate
Location
Bengaluru, India
Employment Type
Full-time
Experience Required
0–2 years
Company
Accenture
Role Overview
The Pharmacovigilance New Associate works within the Life Sciences R&D vertical, supporting drug safety monitoring, adverse event processing, and regulatory compliance activities. The role contributes to ensuring the safety, detection, and reporting of adverse drug reactions across global pharmaceutical programs.
Key Responsibilities
1. Pharmacovigilance Case Processing
Create and manage Individual Case Safety Reports (ICSRs)
Perform case identification and data entry in safety databases
Process adverse event reports from multiple sources
2. Medical Coding & Data Management
Perform MedDRA coding for adverse events
Maintain accuracy in safety database records
Support structured case documentation and tracking
3. Case Submission & Follow-ups
Handle case processing, submission, and follow-up activities
Ensure timely reporting as per client and regulatory requirements
Track case status and ensure completion within timelines
4. Regulatory Compliance
Ensure adherence to global pharmacovigilance guidelines
Follow client-specific protocols and regulatory requirements
Support compliance with safety reporting standards
5. Team Collaboration
Work under supervision with defined scope of work
Collaborate with team members and reporting managers
Participate in structured workflow processes
Required Qualifications
Education
Bachelor of Pharmacy (B.Pharm)
Experience
0–1 year (freshers eligible)
Key Skills Required
Technical Skills
Understanding of pharmacovigilance and drug safety surveillance
Knowledge of adverse event reporting systems
MedDRA coding basics
Familiarity with ICSR processing
Basic understanding of regulatory guidelines
Soft Skills
Strong attention to detail
Ability to follow structured instructions
Problem-solving using predefined guidelines
Team collaboration
Ability to work in rotational shifts
Role Level
Entry-level individual contributor role with supervised responsibilities and limited decision-making scope.
Core Function
This role supports global drug safety operations by processing and documenting adverse event reports, ensuring compliance with pharmacovigilance regulations and maintaining patient safety standards.
About the Company
Accenture is a global professional services company offering technology, consulting, and operations services, including Life Sciences R&D support across pharmacovigilance, clinical, and regulatory domains.
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Remote, India | Siliguri |Illinois :
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Mexico |northeastern :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Sheffield |Oxfordshire :
Witney |Ontario :
Richmond Hill | Australia | North York | Renfrew | Uxbridge | Mississauga |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
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Zaventem |South America :
Peru | Argentina |Brazil :
Brazil | Sao paulo |Attica :
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Auckland |New Zealand :
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Barcelona |Madrid :
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Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
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Japan | Saitama |Tokyo :
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Niš |Bohemia :
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Warsaw |
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