Pharmacovigilance Services Associate
Company: Accenture
Job Title: Pharmacovigilance Services Associate
Job ID: AIOC-S01650564
Job Type: Full-time
Location: Bengaluru, Karnataka, India
Experience Required
Preferred Experience: 1–3 years
Related Openings: 0–2 years (as mentioned in similar Accenture job listings)
Educational Qualification
Candidates should possess any one of the following:
Bachelor of Pharmacy (B.Pharm)
Master of Pharmacy (M.Pharm)
Department
Life Sciences R&D – Pharmacovigilance Operations
Job Summary
Accenture is hiring a Pharmacovigilance Services Associate to join its Life Sciences R&D team. The role focuses on pharmacovigilance operations, drug safety surveillance, and regulatory compliance. The selected candidate will manage adverse event reports, perform MedDRA coding, process Individual Case Safety Reports (ICSRs), and ensure compliance with global pharmacovigilance regulations while supporting leading pharmaceutical clients.
Key Responsibilities
Perform case identification and intake of Individual Case Safety Reports (ICSRs).
Enter and maintain accurate safety data in the pharmacovigilance database.
Perform MedDRA coding for adverse events.
Process, review, and submit safety cases according to client and regulatory guidelines.
Conduct follow-ups for incomplete or pending safety reports.
Ensure compliance with global pharmacovigilance regulations and client requirements.
Maintain high standards of data quality and documentation.
Support drug safety surveillance activities to ensure patient safety.
Required Skills
Pharmacovigilance Operations
Drug Safety Surveillance
ICSR Case Processing
MedDRA Coding
Adverse Event Reporting
Safety Database Management
Regulatory Compliance
Data Entry and Documentation
Attention to Detail
Analytical and Communication Skills
Team Collaboration
Roles and Responsibilities
Resolve routine work-related issues using established procedures and guidelines.
Work closely with team members and report to the direct supervisor.
Complete assigned tasks accurately and within deadlines.
Contribute as an individual team member with a predefined scope of work.
Follow detailed instructions for new assignments.
Be flexible to work in rotational shifts based on business requirements.
Work Environment
Full-time employment.
Team-oriented and collaborative work culture.
Rotational shifts may be required.
Comprehensive onboarding and training provided.
About Accenture
Accenture is a global professional services company specializing in Strategy & Consulting, Technology, Operations, Industry X, and Accenture Song. With over 780,000+ employees serving clients across 120+ countries, Accenture helps organizations transform through digital innovation, cloud, security, and intelligent operations.
Estimated Salary Package
The official job posting does not disclose the salary. Based on current market trends for Pharmacovigilance roles in Bengaluru:
|
Experience |
Estimated Annual CTC |
|---|---|
|
Fresher (0–1 year) |
₹3.8 – ₹5.0 LPA |
|
1–3 years |
₹4.8 – ₹7.2 LPA |
Expected Average CTC: ₹5–7 LPA, depending on experience, interview performance, technical skills, and Accenture's compensation policies.
Who Should Apply
Candidates with:
B.Pharm or M.Pharm qualification.
0–3 years of experience in Pharmacovigilance or Drug Safety.
Knowledge of ICSR processing, MedDRA coding, and adverse event reporting.
Good analytical, communication, and documentation skills.
Willingness to work in rotational shifts.
Location
Bengaluru, Karnataka, India
Employment Type
Full-time
Key Highlights
Opportunity to work with global pharmaceutical and biotechnology clients.
Hands-on experience in Pharmacovigilance Operations and Drug Safety Surveillance.
Exposure to MedDRA coding, ICSR processing, and international regulatory standards.
Career growth opportunities in Life Sciences, Clinical Research, and Pharmacovigilance.
Comprehensive training, certification support, and continuous learning programs.
Inclusive, collaborative, and innovation-driven work environment.
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