Pharmacovigilance Services Associate
Job ID: AIOC-S01619347
Company: Accenture
Location: Bengaluru, India
Employment Type: Full-Time
Functional Area: Pharmacovigilance Operations / Drug Safety
Experience Required: 0–2 years (Freshers with relevant exposure may apply)
Education: B.Pharm / M.Pharm / M.Sc. (Life Sciences or related discipline)
About Accenture
Accenture is a global professional services organization with industry-leading capabilities across digital, cloud, security, and intelligent operations. With a workforce of more than 699,000 professionals across 120+ countries, Accenture partners with organizations to deliver innovation and measurable outcomes. Within the Life Sciences R&D vertical, Accenture supports global biopharmaceutical companies across clinical development, pharmacovigilance, regulatory services, and patient-centric solutions.
Role Overview
The Pharmacovigilance Services Associate will be part of Accenture’s Life Sciences R&D team, supporting global drug safety and pharmacovigilance operations. This role is ideal for early-career professionals seeking hands-on experience in Individual Case Safety Report (ICSR) processing, regulatory compliance, and safety surveillance across global markets. The position plays a key role in ensuring patient safety and regulatory adherence throughout the product lifecycle.
Key Responsibilities
Perform end-to-end ICSR case processing, including case identification, data entry, follow-up, and submission in safety databases.
Conduct MedDRA coding, case quality checks, and documentation in compliance with client procedures and global regulatory requirements.
Manage safety data in accordance with applicable pharmacovigilance guidelines (ICH, GVP, FDA, EMA).
Support timely reporting and follow-up activities for adverse event cases.
Collaborate with team members and supervisors to ensure data accuracy and compliance.
Address routine pharmacovigilance operational issues using established guidelines and standard procedures.
Maintain proper documentation to support audits and inspections.
Work in rotational shifts as per project requirements.
Required Skills & Competencies
Basic understanding of pharmacovigilance and drug safety principles.
Knowledge of ICSR processing workflows and safety databases is preferred.
Strong attention to detail and data accuracy.
Good written and verbal communication skills in English.
Ability to follow standard operating procedures in a regulated environment.
Willingness to learn and grow within global pharmacovigilance operations.
Experience & Qualifications
0 to 2 years of experience in pharmacovigilance, drug safety, or a related life sciences role.
Fresh graduates with relevant academic exposure or internships in pharmacovigilance are encouraged to apply.
Bachelor’s or Master’s degree in Pharmacy or Life Sciences.
Why Join Accenture Life Sciences?
This role offers an excellent entry point into global pharmacovigilance operations, providing exposure to international regulatory frameworks, large-scale safety databases, and cross-functional life sciences teams. Accenture offers structured learning, career growth opportunities, and the ability to contribute to patient safety on a global scale.
Gujarat :
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