Pharmacovigilance Services Associate
Location: Chennai, India
Employment Type: Full-time
Experience Required: 0–2 years
Job ID: AIOC-S01621345
Company Overview
Accenture is a global professional services company specializing in digital, cloud, security, and consulting services across 40+ industries. With a presence in over 120 countries and a workforce of 699,000 professionals, Accenture empowers organizations to transform operations, improve patient outcomes, and deliver innovative healthcare solutions.
Visit: www.accenture.com
Role Overview
The Pharmacovigilance Services Associate will be responsible for end-to-end safety case processing, including case identification, triage, data entry, coding, and submission within regulatory timelines. The role focuses on ensuring compliance with global regulatory standards, accurate documentation in the Global Safety Database, and supporting team activities in a collaborative environment. This position is ideal for early-career professionals in pharmacovigilance, drug safety, or life sciences seeking hands-on experience in ICSR management.
Key Responsibilities
Case Processing & Pharmacovigilance Operations
Identify, create, and process Individual Case Safety Reports (ICSRs) from various sources including intake workflow, client emails, portals, and electronic gateways.
Triage, prioritize, and manage cases according to client SOPs, global regulations, and SLAs.
Perform data entry, medical coding, and narrative writing using MedDRA and WHO Drug dictionaries.
Assess adverse events for seriousness, causality, and regulatory relevance, consulting medical reviewers as required.
Perform duplicate checks, follow-up queries, and ensure completeness of all safety information.
Support submissions for AEs, SAEs, and SUSARs in the Global Safety Database and monitor submission-related issues.
Compliance & Documentation
Ensure all activities comply with regulatory guidelines, SOPs, and client-specific requirements.
Maintain accurate documentation of case processing, training materials, and pharmacovigilance deliverables.
Participate in audits, inspections, and ad-hoc PV projects as needed.
Validate data consistency, correct errors, and follow up for missing or incomplete safety information.
Collaboration & Support
Assist cross-functional teams and liaisons to ensure proper execution of safety processes.
Support knowledge-sharing initiatives and contribute to continuous process improvement.
Coordinate with medical reviewers and other stakeholders for case assessments and query resolution.
Qualifications
Educational Requirements:
Bachelor of Ayurvedic Medicine and Surgery (BAMS) or
Bachelor’s or Master’s Degree in Life Sciences
Experience Required:
0–2 years in pharmacovigilance, drug safety, or clinical data management.
Skills & Competencies:
Understanding of medical terminology and pharmacovigilance principles.
Knowledge of MedDRA and WHO Drug dictionaries preferred.
Proficiency in Microsoft Office and database applications.
Strong medical writing, analytical, and communication skills.
Ability to learn quickly, work independently, and manage multiple priorities.
Attention to detail and adherence to regulatory and compliance standards.
Why Join Accenture
Gain hands-on experience in global pharmacovigilance operations.
Work on end-to-end ICSR processing, data reconciliation, and safety reporting.
Be part of a high-performing team in a collaborative and innovative environment.
Access professional development opportunities, including certifications and training programs.
Build a career with global exposure and opportunities for growth in the healthcare and life sciences domain.
Equal Employment Opportunity
Accenture provides equal employment opportunities to all candidates without regard to age, race, gender, religion, disability, veteran status, or any other legally protected characteristic.
Important Notice: Accenture does not charge applicants for employment. Any request for payment is fraudulent. Report immediately to india.fc.check@accenture.com.
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