Job Title: Pharmacovigilance Services New Associate
Location: Bengaluru, India
Company: Accenture
Job ID: AIOC-S01628166
Employment Type: Full-Time
Experience Required: 0–2 Years
Education Required: MSc / B.Pharm / M.Pharm
Pharmacovigilance Services New Associate | Drug Safety & ICSR Processing
Accenture is hiring a Pharmacovigilance Services New Associate to support drug safety and pharmacovigilance operations within its Life Sciences R&D vertical. This entry-level opportunity is designed for pharmacy and life sciences graduates seeking hands-on experience in Individual Case Safety Report (ICSR) processing, MedDRA coding, and global drug safety compliance.
This role offers exposure to global pharmacovigilance systems and regulatory frameworks while working with leading biopharmaceutical clients.
Role Overview
The Pharmacovigilance Services New Associate will be responsible for managing safety case processing activities including case intake, data entry, coding, follow-up, and submission in accordance with global regulatory guidelines and client-specific procedures.
The role focuses on ensuring patient safety, regulatory compliance, and accurate documentation of adverse events and drug-related issues within pharmacovigilance databases.
Key Responsibilities
Pharmacovigilance Case Processing
Create and manage case identification and data entry for Individual Case Safety Reports (ICSRs).
Perform MedDRA coding for adverse events, indications, and medical history.
Process and validate safety cases in pharmacovigilance databases.
Conduct follow-ups for incomplete case information as required.
Ensure timely submission of safety reports as per global regulatory timelines.
Drug Safety Surveillance
Monitor and assess adverse event data for completeness and accuracy.
Support detection and documentation of drug-related safety concerns.
Adhere to client guidelines and international pharmacovigilance regulations.
Regulatory Compliance
Follow global regulatory requirements related to pharmacovigilance and drug safety reporting.
Maintain documentation integrity and data confidentiality.
Support audit readiness activities within safety operations.
Team Collaboration
Work closely with immediate team members and supervisors.
Solve routine operational problems using established procedures and guidelines.
Operate under structured supervision with clearly defined responsibilities.
Participate in rotational shifts if required by business operations.
Required Qualifications
MSc in Life Sciences OR Bachelor of Pharmacy (B.Pharm) OR Master of Pharmacy (M.Pharm).
0–2 years of experience in Pharmacovigilance or Drug Safety (freshers eligible).
Basic understanding of pharmacovigilance principles and ICSR lifecycle.
Knowledge of MedDRA coding preferred.
Strong attention to detail and data accuracy.
Good written and verbal communication skills.
Preferred Skills
Understanding of global drug safety regulations (FDA, EMA, ICH guidelines).
Familiarity with safety databases and pharmacovigilance workflows.
Ability to manage structured tasks within defined timelines.
Willingness to work in rotational shifts.
Work Environment
This is an individual contributor role within a structured team environment. The position may require working in rotational shifts depending on project requirements.
About Accenture
Accenture is a global professional services organization operating across digital, cloud, security, strategy, consulting, technology, and operations. With a strong presence in Life Sciences and Healthcare, Accenture supports global pharmaceutical companies in clinical research, regulatory services, pharmacovigilance, and patient safety solutions.
The organization serves clients in more than 120 countries and is committed to delivering innovation-driven healthcare solutions.
If you are a pharmacy or life sciences graduate looking to start your career in Pharmacovigilance and Drug Safety Operations, apply now to join Accenture’s Life Sciences R&D team in Bengaluru.
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