Cognizant is Hiring for SPE Pharmacovigilance Positions in Mumbai, Bangalore, and Hyderabad
A Cognizant pharmacovigilance opportunity has emerged for professionals as Cognizant opens SPE Pharmacovigilance positions across multiple cities, including Mumbai, Bangalore, and Hyderabad. This hybrid role is ideal for candidates with at least one year of experience in pharma R&D and clinical documentation.
About the Company
Cognizant is a leading professional services company transforming clients’ business, operating models, and technology architectures for the digital era. With a strong presence in various sectors, including healthcare and life sciences, Cognizant is committed to delivering innovative solutions that enhance operational efficiency and improve patient outcomes.
- Company: Cognizant
- Location: Mumbai / Bangalore / Hyderabad (Hybrid, Day shift)
- Experience: At least 1 year in pharma R&D with clinical/safety documentation
- Qualification: Familiarity with PV case processing; ICSR/dossier basics; DIA/PV certification preferred
- Posted On: 25 September 2026
- Reference ID: cognizant-spe-pv-00069891251
Cognizant Pharmacovigilance Job Description
The SPE Pharmacovigilance position is a Cognizant pharmacovigilance role focused on global medicine safety, including pharmacovigilance case management, safety data handling, clinical documentation, regulatory reporting, and collaboration with clinical safety and quality teams. Candidates will be responsible for end-to-end pharmacovigilance case handling and ensuring compliance with regulatory standards.
Key Responsibilities
- Perform end-to-end pharmacovigilance case handling, including data capture and narrative preparation.
- Review source documents and clinical data to identify relevant safety information.
- Handle spontaneous and solicited adverse event intake, classification, and data entry.
- Conduct medical assessment of individual case safety reports and escalate complex cases when required.
- Prepare regulatory-compliant individual case safety report outputs for electronic submission.
- Monitor case processing workloads and prioritize urgent regulatory timelines.
- Coordinate with clinical operations and quality teams to resolve data inconsistencies and obtain missing information.
- Follow standard operating procedures and global pharmacovigilance guidelines.
Cognizant Pharmacovigilance Eligibility Criteria
- At least 1 year of experience in pharmaceutical research and development activities with exposure to clinical or safety-related documentation.
- Familiarity with pharmacovigilance case processing, including data capture, seriousness assessment, and narrative preparation.
- Strong attention to detail when reviewing medical data, adverse event descriptions, and product information.
- Effective written and verbal communication skills.
- Ability to work in a regulated environment and follow pharmacovigilance procedures.
- Motivation to develop knowledge in pharmacovigilance case processing and related safety sciences.
Required Skills
- Pharmacovigilance Case Processing
- Safety Data Handling
- Clinical Documentation
- Individual Case Safety Reports
- Medical Data Interpretation
- Narrative Preparation
- Dossier Preparation
- Regulatory Reporting
How to Apply
Interested candidates can apply through the official Cognizant careers page:
Conclusion
This Cognizant pharmacovigilance opportunity for the SPE Pharmacovigilance role is an excellent fit for qualified professionals looking to advance their careers in a dynamic environment. Interested candidates are encouraged to apply at the earliest to secure their chance for this role.
