Accenture Hiring Pharma Graduates | PV Services Associate Role
For candidates looking for a Pharmacovigilance Job, Accenture Careers brings an exciting opportunity for pharmacy graduates in the field of drug safety and pharmacovigilance operations. Accenture is hiring a Pharmacovigilance Services Associate in Bengaluru for candidates with a Bachelor of Pharmacy (B Pharm) or Master of Pharmacy (M Pharm) qualification. This role provides an opportunity to work with global life sciences teams and gain experience in safety surveillance, case processing, and regulatory compliance.
- Job Role: Pharmacovigilance Services Associate
- Job Location: Bengaluru, Karnataka
About The Company
Accenture is a global professional services organization providing services across strategy, consulting, technology, operations, and digital transformation. Through Accenture Careers, professionals get opportunities to work on global projects, develop industry-specific skills, and contribute to solutions that improve healthcare outcomes. Accenture’s Life Sciences division supports pharmaceutical and biotechnology companies through services such as clinical research, regulatory support, and pharmacovigilance operations.
Job Description
The selected candidate will work in the Life Sciences R&D vertical and support pharmacovigilance operations related to drug safety monitoring. The role involves identifying and processing safety cases, maintaining safety databases, performing medical coding, and ensuring compliance with global regulatory requirements. This Pharmacovigilance Job is suitable for pharmacy graduates interested in building a career in drug safety, clinical research support, and regulatory compliance.
Key Responsibilities
- Perform pharmacovigilance operations including case identification, data entry, and case processing.
- Manage Individual Case Safety Reports (ICSRs) in safety databases.
- Perform MedDRA coding and ensure accurate documentation of safety information.
- Support case follow-ups and submission activities according to client guidelines.
- Review and analyze adverse event information from clinical trials, healthcare professionals, and patients.
- Ensure compliance with global pharmacovigilance regulations and quality standards.
- Maintain accuracy and data integrity during safety case processing.
- Collaborate with internal teams and supervisors for timely completion of assigned tasks.
Eligibility Criteria
- Education: Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm)
- Experience: Candidates with 1 to 3 years of exposure to pharmacovigilance, drug safety, or life sciences operations will have an advantage.
Required Skills
- Basic understanding of pharmacovigilance principles and drug safety surveillance.
- Knowledge of adverse event reporting and safety case processing.
- Familiarity with MedDRA coding concepts.
- Understanding of regulatory requirements related to pharmaceutical safety.
- Good written and verbal communication skills.
- Strong attention to detail and documentation abilities.
- Ability to analyze information and solve routine problems.
- Willingness to work in rotational shifts if required.



