Pharmacovigilance Services – New Associate
Location: Bengaluru, India
Employment Type: Full-time
Experience Required: 0–2 years
Job ID: AIOC-S01621732
Company Overview
Accenture is a global leader in digital, cloud, security, and consulting services, delivering innovative solutions across 40+ industries. With operations in 120+ countries and a workforce of over 784,000 professionals, Accenture helps organizations transform operations, improve patient safety, and advance healthcare delivery.
Visit: www.accenture.com
Role Overview
The Pharmacovigilance Services New Associate will support end-to-end case processing in drug safety, including identification, triage, data entry, coding, and submission of adverse events (AEs), serious adverse events (SAEs), and SUSARs. This entry-level position is ideal for candidates seeking hands-on experience in global pharmacovigilance operations within a collaborative, compliance-driven environment.
Key Responsibilities
Case Management & Safety Operations
Identify and create Individual Case Safety Reports (ICSRs) in the Global Safety Database from intake workflows, emails, electronic gateways, and other sources.
Perform triage, prioritization, and processing of cases in line with client SOPs, regulatory timelines, and TAT SLAs/KPIs.
Conduct data entry, medical coding, and narrative drafting using MedDRA and WHODrug dictionaries.
Assess adverse events for seriousness, causality, and regulatory relevance, consulting medical reviewers when required.
Validate case data for accuracy, completeness, and compliance with regulatory standards.
Assist in tracking, submission, and distribution of reports; support audits, inspections, and pharmacovigilance projects.
Regulatory Compliance & Documentation
Ensure all activities adhere to global regulatory requirements and client SOPs.
Manage follow-ups for missing information, clarifications, or case corrections.
Document all case-related communications and maintain accurate archival records in the Global Safety Database.
Support paper and electronic unblinding processes as required.
Collaboration & Training Support
Assist in transition activities and cross-training across roles as per business requirements.
Contribute to continuous improvement initiatives in knowledge sharing and process quality.
Coordinate with cross-functional teams to ensure seamless case processing and regulatory compliance.
Qualifications
Educational Requirements:
Bachelor of Ayurvedic Medicine and Surgery (BAMS), or
BSc Nursing, or
Bachelor’s Degree in Life Sciences
Experience Required:
0–2 years in pharmacovigilance, drug safety, or clinical data management.
Skills & Competencies:
Familiarity with pharmacovigilance operations, medical terminology, and safety databases.
Proficiency in Microsoft Office Suite.
Strong communication, analytical, and medical writing skills.
Attention to detail, adherence to regulatory standards, and ability to learn quickly.
Willingness to train across roles and adapt to business needs.
Why Join Accenture
Gain hands-on experience in global pharmacovigilance and drug safety operations.
Work with a leading global consulting and technology company in a high-compliance environment.
Opportunity for career growth and cross-functional exposure in life sciences.
Participate in training, audits, and continuous improvement initiatives.
Access professional development programs, certifications, and mentorship opportunities.
Equal Employment Opportunity
Accenture provides equal employment opportunities to all applicants without regard to age, gender, race, 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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